Variant report

Variant	esv1796351
Chromosome Location	chr1:91722083-91872374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1747)
CpG islands
(count:1098)
Chromatin interactive
region (count:154)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1747 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:91860025-91860071	K562	blood:	n/a	chr1:91860029-91860045
2	ARID3A	chr1:91867503-91867899	K562	blood:	n/a	n/a
3	ARID3A	chr1:91748396-91748636	K562	blood:	n/a	n/a
4	ARID3A	chr1:91870342-91870542	K562	blood:	n/a	n/a
5	ARID3A	chr1:91869593-91869884	K562	blood:	n/a	n/a
6	ARID3A	chr1:91852615-91853313	K562	blood:	n/a	n/a
7	ATF1	chr1:91867732-91867770	K562	blood:	n/a	n/a
8	ATF1	chr1:91852616-91853303	K562	blood:	n/a	n/a
9	ATF1	chr1:91827797-91827927	K562	blood:	n/a	n/a
10	ATF1	chr1:91847427-91847705	K562	blood:	n/a	n/a
11	ATF1	chr1:91774210-91774371	K562	blood:	n/a	n/a
12	ATF2	chr1:91852530-91853203	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr1:91852702-91853157	GM12878	blood:	n/a	n/a
14	ATF2	chr1:91870186-91870726	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr1:91852685-91853210	GM12878	blood:	n/a	n/a
16	ATF3	chr1:91852704-91853188	K562	blood:	n/a	n/a
17	ATF3	chr1:91852516-91853208	A549	lung:	n/a	n/a
18	ATF3	chr1:91852622-91853219	A549	lung:	n/a	n/a
19	ATF3	chr1:91852742-91853159	GM12878	blood:	n/a	n/a
20	ATF3	chr1:91852732-91853164	K562	blood:	n/a	n/a
21	ATF3	chr1:91852721-91853179	HepG2	liver:	n/a	n/a
22	BACH1	chr1:91852610-91853313	K562	blood:	n/a	n/a
23	BACH1	chr1:91869841-91869898	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr1:91870195-91870460	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr1:91748178-91748686	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr1:91748261-91748640	K562	blood:	n/a	n/a
27	BATF	chr1:91852715-91853177	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:91852721-91853175	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:91852709-91853187	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL11A	chr1:91852703-91853193	GM12878	blood:	n/a	n/a
31	BCL3	chr1:91852698-91853197	GM12878	blood:	n/a	n/a
32	BCL3	chr1:91852602-91853230	K562	blood:	n/a	n/a
33	BCL3	chr1:91852704-91853192	GM12878	blood:	n/a	n/a
34	BCL3	chr1:91852678-91853180	K562	blood:	n/a	n/a
35	BCL3	chr1:91852674-91853221	A549	lung:	n/a	n/a
36	BCL3	chr1:91852578-91853236	A549	lung:	n/a	n/a
37	BCLAF1	chr1:91852708-91853188	GM12878	blood:	n/a	n/a
38	BCLAF1	chr1:91852487-91853221	K562	blood:	n/a	n/a
39	BCLAF1	chr1:91852622-91853221	GM12878	blood:	n/a	n/a
40	BCLAF1	chr1:91852666-91853251	K562	blood:	n/a	n/a
41	BHLHE40	chr1:91852719-91853178	HepG2	liver:	n/a	n/a
42	BHLHE40	chr1:91869775-91870404	K562	blood:	n/a	n/a
43	BHLHE40	chr1:91774276-91774286	K562	blood:	n/a	n/a
44	BHLHE40	chr1:91744287-91744311	HepG2	liver:	n/a	n/a
45	BHLHE40	chr1:91852608-91853313	K562	blood:	n/a	n/a
46	BRCA1	chr1:91852613-91853314	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr1:91748269-91748604	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr1:91852608-91853311	HepG2	liver:	n/a	n/a
49	BRCA1	chr1:91852612-91853310	GM12878	blood:	n/a	n/a
50	CBX3	chr1:91773307-91773736	K562	blood:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:91870014-91870064	HEEpiC	esophagus:	n/a
2	chr1:91814033-91814083	Hela-S3	cervix:	n/a
3	chr1:91814033-91814083	AG09319	gingival:	n/a
4	chr1:91870362-91870412	HCT-116	colon:	n/a
5	chr1:91852901-91852951	GM19239	blood:	n/a
6	chr1:91852884-91852934	BJ	skin:	n/a
7	chr1:91869782-91869832	ProgFib	skin:	n/a
8	chr1:91869877-91869927	LNCaP	prostate:	n/a
9	chr1:91871709-91871759	PANC-1	pancreas:	n/a
10	chr1:91871748-91871798	K562	blood:	n/a
11	chr1:91869782-91869832	NHDF-neo	bronchial:	n/a
12	chr1:91754721-91754771	GM12891	blood:	n/a
13	chr1:91853089-91853139	Jurkat	blood:	n/a
14	chr1:91869877-91869927	GM19239	blood:	n/a
15	chr1:91871709-91871759	GM12878	blood:	n/a
16	chr1:91869782-91869832	MCF10A-Er-Src	breast:	n/a
17	chr1:91754721-91754771	SKMC	muscle:	n/a
18	chr1:91852901-91852951	HPAEpiC	pulmonary alveolar:	n/a
19	chr1:91853089-91853139	HCPEpiC	choroid plexus:	n/a
20	chr1:91853024-91853074	Caco-2	colon:	n/a
21	chr1:91814033-91814083	NT2-D1	testis:	n/a
22	chr1:91869877-91869927	GM12878	blood:	n/a
23	chr1:91870389-91870439	ovcar-3	ovarian:	n/a
24	chr1:91852881-91852931	AG09309	skin:	n/a
25	chr1:91870067-91870117	GM12878	blood:	n/a
26	chr1:91870067-91870117	HRCEpiC	kidney:	n/a
27	chr1:91870362-91870412	NT2-D1	testis:	n/a
28	chr1:91852881-91852931	HRCEpiC	kidney:	n/a
29	chr1:91853089-91853139	SK-N-MC	brain:	n/a
30	chr1:91869877-91869927	HUVEC	blood vessel:	n/a
31	chr1:91870450-91870500	LNCaP	prostate:	n/a
32	chr1:91869877-91869927	MCF10A-Er-Src	breast:	n/a
33	chr1:91852884-91852934	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:91869877-91869927	AG04450	lung:	fetal
35	chr1:91871709-91871759	BE2_C	brain:	n/a
36	chr1:91870389-91870439	HRCEpiC	kidney:	n/a
37	chr1:91871709-91871759	IMR90	lung:	fetal
38	chr1:91870450-91870500	HIPEpiC	eye:	n/a
39	chr1:91870067-91870117	ProgFib	skin:	n/a
40	chr1:91754721-91754771	HRCEpiC	kidney:	n/a
41	chr1:91869782-91869832	AG10803	skin:	n/a
42	chr1:91852791-91852841	MCF-7	breast:	n/a
43	chr1:91852791-91852841	NB4	blood:	n/a
44	chr1:91754721-91754771	NHBE	bronchial:	n/a
45	chr1:91870382-91870432	SK-N-MC	brain:	n/a
46	chr1:91870389-91870439	A549	lung:	n/a
47	chr1:91853089-91853139	CMK	blood:	n/a
48	chr1:91870362-91870412	SAEC	small airway:	n/a
49	chr1:91870450-91870500	AoSMC	blood vessel:	n/a
50	chr1:91869782-91869832	HRCEpiC	kidney:	n/a

(count:154 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:91851562..91854585-chr11:85195040..85196753,3	K562	blood:
2	chr1:91852845..91854449-chr1:156186430..156188124,2	K562	blood:
3	chr1:91851415..91854599-chrX:108296235..108299271,9	K562	blood:
4	chr1:91729597..91732468-chr1:91734232..91736198,2	K562	blood:
5	chr1:91852931..91853636-chr8:70601903..70602600,5	MCF-7	breast:
6	chr1:91631181..91632395-chr1:91744047..91745077,4	MCF-7	breast:
7	chr1:91852962..91853614-chrX:108297739..108298319,2	MCF-7	breast:
8	chr1:91851478..91854506-chr2:230045518..230047103,3	K562	blood:
9	chr1:91852326..91853124-chr17:31148951..31149851,3	MCF-7	breast:
10	chr1:91851367..91853065-chr19:24182409..24185198,2	MCF-7	breast:
11	chr1:91852854..91853480-chr8:70601890..70602489,3	MCF-7	breast:
12	chr1:91851478..91854379-chr2:230045518..230047085,3	K562	blood:
13	chr1:91850725..91852999-chr1:91868753..91870397,2	K562	blood:
14	chr1:91858513..91860821-chr1:91867811..91869915,2	K562	blood:
15	chr1:91851628..91854418-chrX:125715189..125716759,2	K562	blood:
16	chr1:91852824..91853644-chrX:108297414..108298331,19	MCF-7	breast:
17	chr1:91851357..91852890-chr2:133010879..133013835,2	K562	blood:
18	chr1:91852378..91853013-chr4:76806710..76807218,2	MCF-7	breast:
19	chr1:91852307..91853117-chr12:127650504..127651422,9	MCF-7	breast:
20	chr1:91851307..91854415-chr20:26188724..26191391,3	K562	blood:
21	chr1:91852809..91854459-chr16:33965483..33967067,2	K562	blood:
22	chr1:91852373..91853105-chr9:79186162..79186710,4	MCF-7	breast:
23	chr1:91871768..91873350-chr1:91886602..91889142,2	K562	blood:
24	chr1:91852880..91853529-chr7:64154..64696,2	MCF-7	breast:
25	chr1:91852330..91853034-chr12:34372628..34373167,11	MCF-7	breast:
26	chr1:91851458..91854565-chrX:108296200..108299331,8	MCF-7	breast:
27	chr1:91786405..91788910-chr1:91799387..91801097,2	K562	blood:
28	chr1:91851381..91853086-chr2:230044008..230045593,2	MCF-7	breast:
29	chr1:91852396..91853586-chr21:9825563..9826775,5	K562	blood:
30	chr1:91852818..91853606-chrX:108297441..108298331,14	MCF-7	breast:
31	chr1:91852994..91853577-chr1:156186039..156186574,2	K562	blood:
32	chr1:91729597..91732468-chr1:91734232..91736198,2	K562	blood:
33	chr1:91745243..91745840-chr1:91867418..91868120,2	MCF-7	breast:
34	chr1:91852355..91852916-chr12:34372634..34373168,4	MCF-7	breast:
35	chr1:91630603..91631513-chr1:91746786..91747465,2	K562	blood:
36	chr1:91852901..91853584-chr8:21456074..21456594,3	MCF-7	breast:
37	chr1:91852396..91852987-chr2:133036550..133037057,2	MCF-7	breast:
38	chr1:91863227..91864915-chr1:91873886..91876249,2	K562	blood:
39	chr1:91852926..91854438-chr8:70600987..70602599,2	K562	blood:
40	chr1:91853063..91854565-chr12:20702914..20704451,2	K562	blood:
41	chr1:91852368..91853008-chr17:31149191..31149753,2	HCT-116	colon:
42	chr1:91840019..91844742-chr1:91867807..91870746,5	K562	blood:
43	chr1:91852287..91853034-chr12:127650621..127651461,9	MCF-7	breast:
44	chr1:91841748..91844457-chr1:91845517..91848039,2	K562	blood:
45	chr1:91747968..91749007-chr1:91867180..91868200,8	MCF-7	breast:
46	chr1:91852480..91853409-chr21:9826549..9827638,3	MCF-7	breast:
47	chr1:91851381..91852904-chr4:76805694..76807215,2	K562	blood:
48	chr1:91852589..91853107-chr3:54356271..54356793,2	MCF-7	breast:
49	chr1:91851362..91853035-chr9:79185170..79186849,5	MCF-7	breast:
50	chr1:91851493..91854339-chr2:224711641..224713931,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HFM1-2	chr1:91794395-91794494	NONHSAT004431
2	lnc-HFM1-2	chr1:91781697-91781741	NONHSAT004431
3	lnc-HFM1-2	chr1:91784850-91784947	NONHSAT004431
4	lnc-HFM1-2	chr1:91788507-91788554	NONHSAT004431
5	lnc-HFM1-2	chr1:91790232-91790323	NONHSAT004431

No data

Variant related genes	Relation type
ENSG00000206817	TF binding region
HFM1	TF binding region
FEN1P1	TF binding region
ENSG00000206817	CpG island
HFM1	CpG island
FEN1P1	CpG island
ENSG00000161847	chromatin interactions
ENSG00000097046	chromatin interactions
ENSG00000207986	chromatin interactions
ENSG00000156194	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000162669	chromatin interactions
ENSG00000264063	chromatin interactions
ENSG00000255652	chromatin interactions
ENSG00000227195	chromatin interactions
ENSG00000241781	chromatin interactions
ENSG00000226958	chromatin interactions
ENSG00000106086	chromatin interactions
ENSG00000239776	chromatin interactions
ENSG00000256642	chromatin interactions

Extended variants
information (count: 5546 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:5546 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs628897	chr1:91722083-91722084	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182088972	chr1:91722214-91722215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529314876	chr1:91722249-91722250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184488425	chr1:91722389-91722390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113595517	chr1:91722395-91722396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569209757	chr1:91722493-91722494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201494178	chr1:91722518-91722519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549651935	chr1:91722554-91722555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181325824	chr1:91722559-91722560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562857359	chr1:91722574-91722575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs578038340	chr1:91722602-91722603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563223631	chr1:91722604-91722605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545301074	chr1:91722608-91722609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531925005	chr1:91722609-91722610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527846407	chr1:91722693-91722694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551714097	chr1:91722694-91722695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549701284	chr1:91722727-91722728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112130356	chr1:91722737-91722738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200038419	chr1:91722743-91722744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200558800	chr1:91722744-91722745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561536478	chr1:91722797-91722798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150072327	chr1:91722818-91722819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549732231	chr1:91722828-91722829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555512928	chr1:91722844-91722845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs642639	chr1:91722873-91722874	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185584673	chr1:91722966-91722967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373668118	chr1:91722994-91722995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190151412	chr1:91723018-91723019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565551518	chr1:91723062-91723063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148619429	chr1:91723063-91723064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182106850	chr1:91723122-91723123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10922991	chr1:91723135-91723136	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs537887895	chr1:91723226-91723227	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186700029	chr1:91723265-91723266	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578065546	chr1:91723283-91723284	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533617429	chr1:91723295-91723296	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560524435	chr1:91723337-91723338	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572700187	chr1:91723402-91723403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs483386	chr1:91723423-91723424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs561599756	chr1:91723425-91723426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532007796	chr1:91723448-91723449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549557239	chr1:91723483-91723484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548164412	chr1:91723506-91723507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564889221	chr1:91723509-91723510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531973940	chr1:91723511-91723512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547095928	chr1:91723590-91723591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566873630	chr1:91723602-91723603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114371878	chr1:91723685-91723686	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
49	rs192315688	chr1:91723701-91723702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114922093	chr1:91723805-91723806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:91717000-91743000	Weak transcription	Fetal Lung	lung
2	chr1:91717200-91741200	Weak transcription	Fetal Kidney	kidney
3	chr1:91717600-91725400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr1:91717800-91723200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:91718400-91722400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr1:91719600-91748400	Weak transcription	Ovary	ovary
7	chr1:91719800-91725200	Weak transcription	Fetal Stomach	stomach
8	chr1:91719800-91736400	Weak transcription	Pancreas	Pancrea
9	chr1:91719800-91748000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr1:91720000-91734000	Weak transcription	Brain Germinal Matrix	brain
11	chr1:91723200-91723400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:91725800-91729000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:91726000-91736400	Weak transcription	Left Ventricle	heart
14	chr1:91729000-91729800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:91729600-91731200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:91729800-91732600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:91729800-91735000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:91731200-91732400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:91731600-91734000	Weak transcription	Fetal Brain Female	brain
20	chr1:91732400-91744200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:91735000-91736000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:91736000-91737800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:91737800-91739800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:91738200-91738800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr1:91738200-91748400	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr1:91738800-91739400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr1:91739200-91740200	Enhancers	HUVEC	blood vessel
28	chr1:91739400-91739600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr1:91739600-91739800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr1:91739600-91739800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:91739800-91743400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:91744000-91744400	Enhancers	K562	blood
33	chr1:91744400-91748400	Weak transcription	K562	blood
34	chr1:91748000-91748400	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr1:91748200-91748400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:91748200-91748400	Enhancers	Adipose Nuclei	Adipose
37	chr1:91748200-91748800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr1:91748200-91748800	Enhancers	Colon Smooth Muscle	Colon
39	chr1:91748200-91749000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr1:91748200-91749000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr1:91748200-91749000	Enhancers	A549	lung
42	chr1:91748400-91748600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:91748400-91748600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:91748400-91748600	Active TSS	Liver	Liver
45	chr1:91748400-91748600	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr1:91748400-91748600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
47	chr1:91748400-91748600	Active TSS	Rectal Smooth Muscle	rectum
48	chr1:91748400-91748600	Active TSS	Osteobl	bone
49	chr1:91748400-91748800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:91748400-91748800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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