Variant report

Variant	nsv946237
Chromosome Location	chr1:144533425-144535801
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:984)
CpG islands
(count:305)
Chromatin interactive
region (count:252)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:984 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:144533334-144534462	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:144535027-144535473	K562	blood:	n/a	n/a
3	ARID3A	chr1:144535206-144535581	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:144532762-144534541	K562	blood:	n/a	n/a
5	ATF1	chr1:144533100-144534496	K562	blood:	n/a	n/a
6	ATF1	chr1:144535220-144535590	K562	blood:	n/a	n/a
7	ATF2	chr1:144533458-144534609	GM12878	blood:	n/a	n/a
8	ATF2	chr1:144533212-144534565	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr1:144533382-144534573	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:144533459-144534584	GM12878	blood:	n/a	n/a
11	ATF3	chr1:144533311-144534469	A549	lung:	n/a	chr1:144533784-144533797 chr1:144533946-144533955 chr1:144533783-144533798
12	ATF3	chr1:144533542-144534429	K562	blood:	n/a	chr1:144533784-144533797 chr1:144533946-144533955 chr1:144533783-144533798
13	ATF3	chr1:144533135-144534621	A549	lung:	n/a	chr1:144533784-144533797 chr1:144533946-144533955 chr1:144533783-144533798
14	ATF3	chr1:144533095-144534612	K562	blood:	n/a	chr1:144533784-144533797 chr1:144533946-144533955 chr1:144533783-144533798
15	BACH1	chr1:144534872-144535121	K562	blood:	n/a	n/a
16	BACH1	chr1:144532809-144534499	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:144532785-144534560	K562	blood:	n/a	n/a
18	BATF	chr1:144533969-144534491	GM12878	blood:	n/a	n/a
19	BATF	chr1:144533655-144534561	GM12878	blood:	n/a	n/a
20	BCL11A	chr1:144533943-144534432	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr1:144533853-144534617	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:144533682-144534616	GM12878	blood:	n/a	chr1:144533775-144533783
23	BCL11A	chr1:144533840-144534502	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL3	chr1:144533846-144534501	K562	blood:	n/a	n/a
25	BCL3	chr1:144533167-144534598	A549	lung:	n/a	chr1:144533775-144533783
26	BCL3	chr1:144533414-144534775	K562	blood:	n/a	chr1:144533775-144533783
27	BCL3	chr1:144533245-144534596	A549	lung:	n/a	chr1:144533775-144533783
28	BCL3	chr1:144533885-144534574	GM12878	blood:	n/a	n/a
29	BCL3	chr1:144533830-144534436	GM12878	blood:	n/a	n/a
30	BCLAF1	chr1:144533324-144534619	GM12878	blood:	n/a	chr1:144533775-144533783
31	BCLAF1	chr1:144532781-144534769	K562	blood:	n/a	chr1:144533775-144533783
32	BCLAF1	chr1:144533122-144534615	K562	blood:	n/a	chr1:144533775-144533783
33	BCLAF1	chr1:144533644-144534620	GM12878	blood:	n/a	chr1:144533775-144533783
34	BHLHE40	chr1:144533305-144534550	GM12878	blood:	n/a	n/a
35	BHLHE40	chr1:144533255-144534490	HepG2	liver:	n/a	n/a
36	BHLHE40	chr1:144535260-144535417	GM12878	blood:	n/a	n/a
37	BHLHE40	chr1:144533242-144534538	K562	blood:	n/a	n/a
38	BHLHE40	chr1:144535220-144535584	K562	blood:	n/a	n/a
39	BRCA1	chr1:144535232-144535463	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr1:144533161-144534406	HepG2	liver:	n/a	n/a
41	BRCA1	chr1:144533309-144534465	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr1:144533728-144534396	GM12878	blood:	n/a	n/a
43	BRF2	chr1:144534035-144534449	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr1:144533427-144534452	HCT-116	colon:	n/a	n/a
45	CBX3	chr1:144532664-144534621	K562	blood:	n/a	n/a
46	CBX3	chr1:144532555-144534695	K562	blood:	n/a	n/a
47	CCNT2	chr1:144533654-144534463	K562	blood:	n/a	chr1:144533946-144533955
48	CEBPB	chr1:144533515-144534496	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr1:144533417-144534515	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr1:144533627-144534439	A549	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144533861-144533911	PFSK-1	brain:	n/a
2	chr1:144533844-144533894	IMR90	lung:	fetal
3	chr1:144534187-144534237	AG04450	lung:	fetal
4	chr1:144534187-144534237	HPAEpiC	pulmonary alveolar:	n/a
5	chr1:144533778-144533828	ECC-1	luminal epithelium:	n/a
6	chr1:144533778-144533828	SK-N-MC	brain:	n/a
7	chr1:144533844-144533894	HEEpiC	esophagus:	n/a
8	chr1:144533844-144533894	K562	blood:	n/a
9	chr1:144533951-144534001	Hepatocyte	liver:	n/a
10	chr1:144534187-144534237	HCM	heart:	n/a
11	chr1:144533778-144533828	PANC-1	pancreas:	n/a
12	chr1:144533951-144534001	SK-N-SH_RA	brain:	n/a
13	chr1:144533861-144533911	HCM	heart:	n/a
14	chr1:144533778-144533828	NT2-D1	testis:	n/a
15	chr1:144533844-144533894	NHBE	bronchial:	n/a
16	chr1:144534187-144534237	ECC-1	luminal epithelium:	n/a
17	chr1:144533844-144533894	PrEC	prostate:	n/a
18	chr1:144533844-144533894	NH-A	brain:	n/a
19	chr1:144533951-144534001	LNCaP	prostate:	n/a
20	chr1:144533951-144534001	AoSMC	blood vessel:	n/a
21	chr1:144534187-144534237	ProgFib	skin:	n/a
22	chr1:144533951-144534001	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:144533778-144533828	Jurkat	blood:	n/a
24	chr1:144533861-144533911	SKMC	muscle:	n/a
25	chr1:144533778-144533828	HepG2	liver:	n/a
26	chr1:144533861-144533911	MCF-7	breast:	n/a
27	chr1:144534187-144534237	GM12892	blood:	n/a
28	chr1:144533844-144533894	H1-hESC	embryonic stem cell:	embryo
29	chr1:144533861-144533911	AG09309	skin:	n/a
30	chr1:144533861-144533911	IMR90	lung:	fetal
31	chr1:144533951-144534001	HepG2	liver:	n/a
32	chr1:144533951-144534001	HCF	heart:	n/a
33	chr1:144533844-144533894	AG04450	lung:	fetal
34	chr1:144533951-144534001	HCM	heart:	n/a
35	chr1:144533844-144533894	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:144533861-144533911	PANC-1	pancreas:	n/a
37	chr1:144534187-144534237	HRE	kidney:	n/a
38	chr1:144533951-144534001	HMEC	breast:	n/a
39	chr1:144533778-144533828	HCT-116	colon:	n/a
40	chr1:144534187-144534237	HRCEpiC	kidney:	n/a
41	chr1:144533951-144534001	GM06990	blood:	n/a
42	chr1:144534187-144534237	LNCaP	prostate:	n/a
43	chr1:144533951-144534001	NH-A	brain:	n/a
44	chr1:144533778-144533828	PFSK-1	brain:	n/a
45	chr1:144534187-144534237	Hepatocyte	liver:	n/a
46	chr1:144534187-144534237	HNPCEpiC	eye:	n/a
47	chr1:144533844-144533894	GM06990	blood:	n/a
48	chr1:144533951-144534001	MCF-7	breast:	n/a
49	chr1:144533861-144533911	ECC-1	luminal epithelium:	n/a
50	chr1:144533951-144534001	MCF10A-Er-Src	breast:	n/a

(count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr1:144533606..144534311-chr10:112631501..112632009,2	Hela-S3	cervix:
2	chr1:144533574..144534118-chr13:52027490..52028216,2	Hela-S3	cervix:
3	chr1:144534046..144534703-chr8:119123617..119124191,2	Hela-S3	cervix:
4	chr1:144532970..144534328-chr1:149194157..149195181,24	Hela-S3	cervix:
5	chr1:17221575..17223414-chr1:144532305..144534142,2	K562	blood:
6	chr1:120428374..120430929-chr1:144532739..144535945,3	K562	blood:
7	chr1:144534235..144535874-chr1:145017887..145020000,2	K562	blood:
8	chr1:144534740..144535279-chr2:5765424..5766032,2	Hela-S3	cervix:
9	chr1:144534065..144535931-chr1:145036199..145038965,3	K562	blood:
10	chr1:144533839..144534637-chr9:130374190..130374874,2	Hela-S3	cervix:
11	chr1:144534225..144536279-chr2:5765333..5766332,12	MCF-7	breast:
12	chr1:144534103..144535886-chr1:148549842..148552268,2	K562	blood:
13	chr1:144534129..144535866-chr1:149816096..149818142,2	K562	blood:
14	chr1:144533649..144534390-chr17:79479085..79479816,3	Hela-S3	cervix:
15	chr1:144533777..144534760-chr3:20227219..20227949,2	Hela-S3	cervix:
16	chr1:51701826..51702360-chr1:144533729..144534245,2	Hela-S3	cervix:
17	chr1:144534120..144534744-chr11:62648041..62648567,2	Hela-S3	cervix:
18	chr1:144534089..144535693-chr1:145093143..145095512,2	K562	blood:
19	chr1:70876503..70877021-chr1:144533689..144534211,2	Hela-S3	cervix:
20	chr1:144533638..144534274-chr19:15217961..15218528,2	Hela-S3	cervix:
21	chr1:144535146..144535890-chr2:5765818..5766338,2	K562	blood:
22	chr1:144533785..144534480-chr7:149535088..149535984,2	Hela-S3	cervix:
23	chr1:144529973..144534952-chr1:149221200..149225268,6	MCF-7	breast:
24	chr1:144533513..144534190-chr17:8093096..8093745,2	Hela-S3	cervix:
25	chr1:144532329..144535680-chr1:145012343..145016063,5	K562	blood:
26	chr1:144533852..144534586-chr1:184377390..184378370,3	Hela-S3	cervix:
27	chr1:144533704..144534341-chr1:167906119..167906857,2	Hela-S3	cervix:
28	chr1:144533696..144534515-chr1:205180497..205181167,2	Hela-S3	cervix:
29	chr1:23857219..23858177-chr1:144534191..144535004,2	Hela-S3	cervix:
30	chr1:144533750..144534472-chr15:34516659..34517532,2	Hela-S3	cervix:
31	chr1:144527325..144537192-chr1:149221188..149227183,106	K562	blood:
32	chr1:144533671..144534251-chr12:77157377..77158064,2	Hela-S3	cervix:
33	chr1:144533960..144534647-chr17:16342053..16342570,2	Hela-S3	cervix:
34	chr1:144533652..144534300-chr12:56552105..56553643,4	Hela-S3	cervix:
35	chr1:144533948..144534472-chr20:55204216..55204868,2	Hela-S3	cervix:
36	chr1:144534120..144534663-chr12:8185207..8185847,2	Hela-S3	cervix:
37	chr1:144533647..144534246-chr11:63953498..63954179,2	Hela-S3	cervix:
38	chr1:144531419..144535550-chr1:144535680..144537303,4	MCF-7	breast:
39	chr1:144526732..144539178-chr1:149221186..149225476,28	MCF-7	breast:
40	chr1:144533640..144534142-chr11:64901928..64902515,2	Hela-S3	cervix:
41	chr1:144533772..144534662-chr2:27434968..27435566,3	Hela-S3	cervix:
42	chr1:17221440..17223414-chr1:144532305..144534146,3	K562	blood:
43	chr1:28974690..28975488-chr1:144533795..144534626,3	HCT-116	colon:
44	chr1:36235021..36235536-chr1:144534159..144534971,2	Hela-S3	cervix:
45	chr1:144533474..144535721-chr1:145039954..145042434,2	K562	blood:
46	chr1:144533565..144534214-chr12:107486718..107487481,2	Hela-S3	cervix:
47	chr1:117602451..117603365-chr1:144533561..144534304,2	Hela-S3	cervix:
48	chr1:144530771..144535863-chr1:144988447..145007040,21	K562	blood:
49	chr1:144532709..144537146-chr1:146553385..146558827,17	K562	blood:
50	chr1:144533640..144534222-chr5:180649728..180650375,2	Hela-S3	cervix:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL592284.1-2	chr1:144534038-144534457	NONHSAT005812

No data

Variant related genes	Relation type
RNU1-59P	TF binding region
RNU1-59P	CpG island
ENSG00000151881	chromatin interactions
ENSG00000048162	chromatin interactions
ENSG00000117054	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000234028	chromatin interactions
ENSG00000150593	chromatin interactions
ENSG00000196204	chromatin interactions
ENSG00000207005	chromatin interactions
ENSG00000136854	chromatin interactions
ENSG00000160193	chromatin interactions
ENSG00000223473	chromatin interactions
ENSG00000087299	chromatin interactions
ENSG00000138600	chromatin interactions
ENSG00000185825	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000164040	chromatin interactions
ENSG00000243452	chromatin interactions
ENSG00000143578	chromatin interactions
ENSG00000226446	chromatin interactions
ENSG00000108264	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000230832	chromatin interactions
ENSG00000197019	chromatin interactions
ENSG00000236943	chromatin interactions
ENSG00000102996	chromatin interactions
ENSG00000143458	chromatin interactions
ENSG00000272755	chromatin interactions
ENSG00000186020	chromatin interactions
ENSG00000065970	chromatin interactions
ENSG00000178607	chromatin interactions
ENSG00000128272	chromatin interactions
ENSG00000138085	chromatin interactions
ENSG00000180185	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000102144	chromatin interactions
ENSG00000112305	chromatin interactions
ENSG00000139722	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000146063	chromatin interactions
ENSG00000268172	chromatin interactions
ENSG00000108511	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000171067	chromatin interactions
ENSG00000272426	chromatin interactions
ENSG00000175581	chromatin interactions
ENSG00000231721	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000134697	chromatin interactions
ENSG00000164087	chromatin interactions
ENSG00000092841	chromatin interactions
ENSG00000123091	chromatin interactions
ENSG00000135316	chromatin interactions
ENSG00000119912	chromatin interactions
ENSG00000270141	chromatin interactions
ENSG00000234684	chromatin interactions
ENSG00000132466	chromatin interactions
ENSG00000160194	chromatin interactions
ENSG00000167280	chromatin interactions
ENSG00000168040	chromatin interactions
ENSG00000136451	chromatin interactions
ENSG00000198231	chromatin interactions
ENSG00000223501	chromatin interactions
ENSG00000063177	chromatin interactions
ENSG00000175061	chromatin interactions
ENSG00000186908	chromatin interactions
ENSG00000206344	chromatin interactions
ENSG00000087510	chromatin interactions
ENSG00000172270	chromatin interactions
ENSG00000272822	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000116863	chromatin interactions
ENSG00000171530	chromatin interactions
ENSG00000151422	chromatin interactions
ENSG00000182872	chromatin interactions
ENSG00000259708	chromatin interactions
ENSG00000230470	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000261202	chromatin interactions
ENSG00000100219	chromatin interactions
ENSG00000143158	chromatin interactions
ENSG00000232956	chromatin interactions
ENSG00000203497	chromatin interactions
ENSG00000063854	chromatin interactions
ENSG00000203814	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000231500	chromatin interactions
ENSG00000163399	chromatin interactions
ENSG00000207205	chromatin interactions
ENSG00000256982	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000125375	chromatin interactions
ENSG00000170852	chromatin interactions
ENSG00000125775	chromatin interactions
ENSG00000266173	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000252826	chromatin interactions
ENSG00000273071	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000166439	chromatin interactions
ENSG00000124198	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000197622	chromatin interactions
ENSG00000136159	chromatin interactions
ENSG00000122884	chromatin interactions
ENSG00000105887	chromatin interactions
ENSG00000126088	chromatin interactions
ENSG00000237188	chromatin interactions
ENSG00000140403	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000127483	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000269501	chromatin interactions
ENSG00000067082	chromatin interactions
ENSG00000143401	chromatin interactions
ENSG00000196544	chromatin interactions
ENSG00000174446	chromatin interactions
ENSG00000168439	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000177666	chromatin interactions
ENSG00000115963	chromatin interactions
ENSG00000262420	chromatin interactions
ENSG00000131791	chromatin interactions
ENSG00000169189	chromatin interactions
ENSG00000134001	chromatin interactions
ENSG00000176619	chromatin interactions
ENSG00000026025	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000185947	chromatin interactions
ENSG00000113387	chromatin interactions
ENSG00000082269	chromatin interactions
ENSG00000007968	chromatin interactions
ENSG00000146066	chromatin interactions
ENSG00000250220	chromatin interactions
ENSG00000100354	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000267751	chromatin interactions
ENSG00000108588	chromatin interactions
ENSG00000134717	chromatin interactions
ENSG00000166441	chromatin interactions
ENSG00000105137	chromatin interactions
ENSG00000242663	chromatin interactions
ENSG00000204856	chromatin interactions
ENSG00000120742	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000106479	chromatin interactions
ENSG00000143164	chromatin interactions
ENSG00000262001	chromatin interactions
ENSG00000183891	chromatin interactions
ENSG00000257548	chromatin interactions
ENSG00000007944	chromatin interactions
ENSG00000236200	chromatin interactions
ENSG00000159208	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000108256	chromatin interactions
ENSG00000153208	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000079999	chromatin interactions
ENSG00000085872	chromatin interactions
ENSG00000136144	chromatin interactions
ENSG00000115073	chromatin interactions
ENSG00000245888	chromatin interactions
ENSG00000113580	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000270022	chromatin interactions
ENSG00000138459	chromatin interactions
ENSG00000083838	chromatin interactions
ENSG00000120306	chromatin interactions
ENSG00000091527	chromatin interactions
ENSG00000117862	chromatin interactions
ENSG00000124193	chromatin interactions
ENSG00000179119	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000170633	chromatin interactions
ENSG00000133398	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000100227	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000076003	chromatin interactions
ENSG00000168010	chromatin interactions
ENSG00000008405	chromatin interactions
ENSG00000181991	chromatin interactions
ENSG00000183598	chromatin interactions
ENSG00000212456	chromatin interactions
ENSG00000128463	chromatin interactions
ENSG00000271991	chromatin interactions
ENSG00000252656	chromatin interactions
ENSG00000147403	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000171863	chromatin interactions
ENSG00000162298	chromatin interactions
ENSG00000145996	chromatin interactions
ENSG00000133059	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000272993	chromatin interactions
ENSG00000072121	chromatin interactions
ENSG00000115415	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000207349	chromatin interactions
ENSG00000138074	chromatin interactions
ENSG00000113441	chromatin interactions
ENSG00000184277	chromatin interactions
ENSG00000092853	chromatin interactions
ENSG00000202496	chromatin interactions
ENSG00000136143	chromatin interactions
ENSG00000144895	chromatin interactions
ENSG00000149257	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000111276	chromatin interactions
ENSG00000132142	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000126777	chromatin interactions
ENSG00000123908	chromatin interactions
ENSG00000147123	chromatin interactions
ENSG00000167460	chromatin interactions
ENSG00000173207	chromatin interactions
ENSG00000182197	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000092531	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000111231	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000134287	chromatin interactions
ENSG00000120738	chromatin interactions
ENSG00000021776	chromatin interactions
ENSG00000116830	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000160051	chromatin interactions
ENSG00000267598	chromatin interactions
ENSG00000089053	chromatin interactions
ENSG00000146963	chromatin interactions
ENSG00000153094	chromatin interactions
ENSG00000120093	chromatin interactions
ENSG00000232151	chromatin interactions
ENSG00000118515	chromatin interactions
ENSG00000185670	chromatin interactions
ENSG00000233527	chromatin interactions
ENSG00000100554	chromatin interactions
ENSG00000144848	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000113838	chromatin interactions
ENSG00000125753	chromatin interactions
ENSG00000129810	chromatin interactions
ENSG00000268032	chromatin interactions

Extended variants
information (count: 139 )
Associated
traits (count: 165 )

Variant overlapped rSNPs/rCNVs (count:139 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587634176	chr1:144533459-144533460	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	40 gene(s)	Overlapped CNVs	n/a
2	rs138798553	chr1:144533477-144533478	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	40 gene(s)	Overlapped CNVs	n/a
3	rs66523280	chr1:144533512-144533513	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	43 gene(s)	Overlapped CNVs	n/a
4	rs10596116	chr1:144533514-144533515	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	44 gene(s)	Overlapped CNVs	n/a
5	rs11261232	chr1:144533625-144533626	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	74 gene(s)	Overlapped CNVs	mRNA abundance
6	rs2455992	chr1:144533632-144533633	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	89 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs2940060	chr1:144533647-144533648	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	100 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs587775643	chr1:144533657-144533658	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	110 gene(s)	Overlapped CNVs	n/a
9	rs557020	chr1:144533660-144533661	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	110 gene(s)	Overlapped CNVs	n/a
10	rs369098126	chr1:144533661-144533662	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	110 gene(s)	Overlapped CNVs	n/a
11	rs375014777	chr1:144533672-144533673	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	115 gene(s)	Overlapped CNVs	n/a
12	rs513229	chr1:144533700-144533701	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	130 gene(s)	Overlapped CNVs	n/a
13	rs113421110	chr1:144533704-144533705	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	134 gene(s)	Overlapped CNVs	n/a
14	rs372660076	chr1:144533709-144533710	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	135 gene(s)	Overlapped CNVs	n/a
15	rs513171	chr1:144533715-144533716	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	135 gene(s)	Overlapped CNVs	n/a
16	rs587755474	chr1:144533729-144533730	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	149 gene(s)	Overlapped CNVs	n/a
17	rs587645588	chr1:144533733-144533734	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	152 gene(s)	Overlapped CNVs	n/a
18	rs587710521	chr1:144533759-144533760	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	166 gene(s)	Overlapped CNVs	n/a
19	rs386635170	chr1:144533763-144533764	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	166 gene(s)	Overlapped CNVs	n/a
20	rs587663441	chr1:144533767-144533768	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region	166 gene(s)	Overlapped CNVs	n/a
21	rs587718620	chr1:144533782-144533783	Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	173 gene(s)	Overlapped CNVs	n/a
22	rs587597521	chr1:144533810-144533811	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	183 gene(s)	Overlapped CNVs	n/a
23	rs587671559	chr1:144533841-144533842	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	190 gene(s)	Overlapped CNVs	n/a
24	rs511585	chr1:144533845-144533846	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	191 gene(s)	Overlapped CNVs	n/a
25	rs189041659	chr1:144533846-144533847	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	191 gene(s)	Overlapped CNVs	n/a
26	rs3009852	chr1:144533849-144533850	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	196 gene(s)	Overlapped CNVs	n/a
27	rs2938630	chr1:144533886-144533887	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	207 gene(s)	Overlapped CNVs	n/a
28	rs587674333	chr1:144533894-144533895	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	209 gene(s)	Overlapped CNVs	n/a
29	rs181685591	chr1:144533897-144533898	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	209 gene(s)	Overlapped CNVs	n/a
30	rs587626792	chr1:144533908-144533909	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	209 gene(s)	Overlapped CNVs	n/a
31	rs587711303	chr1:144533915-144533916	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	209 gene(s)	Overlapped CNVs	n/a
32	rs112299833	chr1:144533930-144533931	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	209 gene(s)	Overlapped CNVs	n/a
33	rs510680	chr1:144533972-144533973	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	218 gene(s)	Overlapped CNVs	n/a
34	rs4950188	chr1:144533982-144533983	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	220 gene(s)	Overlapped CNVs	n/a
35	rs61803041	chr1:144533984-144533985	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	220 gene(s)	Overlapped CNVs	n/a
36	rs587775390	chr1:144533985-144533986	Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	220 gene(s)	Overlapped CNVs	n/a
37	rs186387564	chr1:144534002-144534003	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	220 gene(s)	Overlapped CNVs	n/a
38	rs79622576	chr1:144534021-144534022	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	221 gene(s)	Overlapped CNVs	n/a
39	rs12407184	chr1:144534025-144534026	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	221 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs74711042	chr1:144534027-144534028	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	221 gene(s)	Overlapped CNVs	n/a
41	rs76950890	chr1:144534038-144534039	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	222 gene(s)	Overlapped CNVs	n/a
42	rs11261234	chr1:144534045-144534046	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	221 gene(s)	Overlapped CNVs	n/a
43	rs587719348	chr1:144534068-144534069	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	222 gene(s)	Overlapped CNVs	n/a
44	rs76270464	chr1:144534076-144534077	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	222 gene(s)	Overlapped CNVs	n/a
45	rs386635171	chr1:144534082-144534083	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	222 gene(s)	Overlapped CNVs	n/a
46	rs10737112	chr1:144534083-144534084	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	222 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs587652272	chr1:144534084-144534085	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	222 gene(s)	Overlapped CNVs	n/a
48	rs587703546	chr1:144534085-144534086	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	222 gene(s)	Overlapped CNVs	n/a
49	rs587763241	chr1:144534087-144534088	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	222 gene(s)	Overlapped CNVs	n/a
50	rs587638939	chr1:144534089-144534090	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	222 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:165)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Cancer	17440070	CNVD

Chromatin state (count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144528800-144533800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:144529400-144533800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:144530800-144533600	Strong transcription	HSMM	muscle
4	chr1:144532800-144533800	Flanking Active TSS	K562	blood
5	chr1:144532800-144534400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:144532800-144534600	ZNF genes & repeats	Spleen	Spleen
7	chr1:144532800-144534800	ZNF genes & repeats	Right Atrium	heart
8	chr1:144533000-144533600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:144533000-144533600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:144533000-144533600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
11	chr1:144533000-144533600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
12	chr1:144533000-144533600	Flanking Active TSS	Brain Anterior Caudate	brain
13	chr1:144533000-144534200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
14	chr1:144533000-144534400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:144533200-144533600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr1:144533200-144533600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr1:144533200-144533600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr1:144533200-144533600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr1:144533200-144533600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr1:144533200-144533600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr1:144533200-144533600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
24	chr1:144533200-144533600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Liver	Liver
26	chr1:144533200-144533600	Flanking Active TSS	Brain Angular Gyrus	brain
27	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
28	chr1:144533200-144533600	Flanking Active TSS	Brain Substantia Nigra	brain
29	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
30	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
31	chr1:144533200-144533600	Flanking Bivalent TSS/Enh	Fetal Heart	heart
32	chr1:144533200-144533600	Flanking Active TSS	A549	lung
33	chr1:144533200-144533600	Flanking Active TSS	Hela-S3	cervix
34	chr1:144533200-144533800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
35	chr1:144533200-144533800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:144533200-144533800	Flanking Active TSS	Fetal Brain Female	brain
37	chr1:144533200-144533800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
38	chr1:144533200-144534000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:144533200-144534000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:144533200-144534000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:144533200-144534000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
42	chr1:144533200-144534200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
43	chr1:144533200-144534200	Flanking Active TSS	HMEC	breast
44	chr1:144533200-144534200	Bivalent/Poised TSS	Osteobl	bone
45	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
46	chr1:144533200-144534400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr1:144533200-144534400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr1:144533200-144534400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
49	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:144533200-144534400	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain

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