Variant report

Variant	nsv461762
Chromosome Location	chr1:67551209-67648460
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1167)
CpG islands
(count:1403)
Chromatin interactive
region (count:41)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1167 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:67568179-67568416	K562	blood:	n/a	n/a
2	ARID3A	chr1:67637355-67637358	K562	blood:	n/a	n/a
3	ARID3A	chr1:67598888-67599189	K562	blood:	n/a	chr1:67598965-67598981
4	ARID3A	chr1:67628723-67628906	K562	blood:	n/a	n/a
5	ARID3A	chr1:67607315-67607754	K562	blood:	n/a	n/a
6	ARID3A	chr1:67614928-67615146	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:67610363-67610693	K562	blood:	n/a	n/a
8	ARID3A	chr1:67610445-67610596	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:67635465-67635943	HepG2	liver:	n/a	n/a
10	ATF1	chr1:67592176-67592449	K562	blood:	n/a	n/a
11	ATF1	chr1:67555677-67555833	K562	blood:	n/a	n/a
12	ATF2	chr1:67637193-67638222	GM12878	blood:	n/a	n/a
13	ATF2	chr1:67637237-67638138	GM12878	blood:	n/a	n/a
14	ATF2	chr1:67631760-67632326	GM12878	blood:	n/a	n/a
15	ATF2	chr1:67628574-67628974	GM12878	blood:	n/a	n/a
16	ATF2	chr1:67628561-67629007	GM12878	blood:	n/a	n/a
17	ATF2	chr1:67631737-67632279	GM12878	blood:	n/a	n/a
18	ATF2	chr1:67578090-67578663	GM12878	blood:	n/a	n/a
19	ATF3	chr1:67628601-67629028	K562	blood:	n/a	n/a
20	BACH1	chr1:67563094-67563309	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr1:67628675-67629039	GM12878	blood:	n/a	chr1:67628846-67628857
22	BATF	chr1:67628566-67629084	GM12878	blood:	n/a	chr1:67628846-67628857
23	BATF	chr1:67631842-67632208	GM12878	blood:	n/a	chr1:67632018-67632027
24	BATF	chr1:67631328-67631606	GM12878	blood:	n/a	n/a
25	BATF	chr1:67637203-67637420	GM12878	blood:	n/a	n/a
26	BATF	chr1:67624880-67625275	GM12878	blood:	n/a	chr1:67625115-67625126
27	BATF	chr1:67637530-67638035	GM12878	blood:	n/a	n/a
28	BATF	chr1:67637467-67638069	GM12878	blood:	n/a	chr1:67638039-67638049 chr1:67638043-67638053
29	BATF	chr1:67641233-67641477	GM12878	blood:	n/a	chr1:67641364-67641375
30	BATF	chr1:67631800-67632247	GM12878	blood:	n/a	chr1:67632018-67632027
31	BCL11A	chr1:67628595-67629096	GM12878	blood:	n/a	n/a
32	BCL11A	chr1:67616715-67616943	GM12878	blood:	n/a	n/a
33	BCL11A	chr1:67637566-67638070	GM12878	blood:	n/a	chr1:67638042-67638051 chr1:67638041-67638050
34	BCL11A	chr1:67631872-67632147	GM12878	blood:	n/a	chr1:67632104-67632113 chr1:67631991-67632000
35	BCL11A	chr1:67624881-67625227	GM12878	blood:	n/a	n/a
36	BCL11A	chr1:67631809-67632211	GM12878	blood:	n/a	chr1:67632104-67632113 chr1:67631991-67632000
37	BCL11A	chr1:67624928-67625230	GM12878	blood:	n/a	n/a
38	BCL3	chr1:67631792-67632254	GM12878	blood:	n/a	chr1:67632104-67632113 chr1:67631991-67632000
39	BCL3	chr1:67637480-67638116	GM12878	blood:	n/a	chr1:67638042-67638051 chr1:67638041-67638050
40	BCLAF1	chr1:67631786-67632388	GM12878	blood:	n/a	chr1:67632104-67632113 chr1:67631991-67632000
41	BCLAF1	chr1:67631729-67632305	GM12878	blood:	n/a	chr1:67632104-67632113 chr1:67631991-67632000
42	BCLAF1	chr1:67637250-67638018	GM12878	blood:	n/a	n/a
43	BCLAF1	chr1:67637349-67638095	GM12878	blood:	n/a	chr1:67638042-67638051 chr1:67638041-67638050
44	BCLAF1	chr1:67614765-67615272	GM12878	blood:	n/a	n/a
45	BCLAF1	chr1:67578029-67578650	GM12878	blood:	n/a	n/a
46	BHLHE40	chr1:67631789-67632304	GM12878	blood:	n/a	n/a
47	BHLHE40	chr1:67616836-67616921	GM12878	blood:	n/a	n/a
48	BHLHE40	chr1:67637186-67638108	GM12878	blood:	n/a	n/a
49	BHLHE40	chr1:67614800-67615225	GM12878	blood:	n/a	n/a
50	BHLHE40	chr1:67640355-67640795	GM12878	blood:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:67631214-67631264	SK-N-SH_RA	brain:	n/a
2	chr1:67600172-67600222	GM12878	blood:	n/a
3	chr1:67562326-67562376	HCM	heart:	n/a
4	chr1:67636724-67636774	BJ	skin:	n/a
5	chr1:67600311-67600361	PFSK-1	brain:	n/a
6	chr1:67632028-67632078	Hela-S3	cervix:	n/a
7	chr1:67597928-67597978	NH-A	brain:	n/a
8	chr1:67600428-67600478	IMR90	lung:	fetal
9	chr1:67632028-67632078	MCF-7	breast:	n/a
10	chr1:67600687-67600737	BJ	skin:	n/a
11	chr1:67603174-67603224	BJ	skin:	n/a
12	chr1:67600835-67600885	ECC-1	luminal epithelium:	n/a
13	chr1:67604092-67604142	AG09319	gingival:	n/a
14	chr1:67600687-67600737	HRE	kidney:	n/a
15	chr1:67594788-67594838	U87	brain:	n/a
16	chr1:67632028-67632078	SKMC	muscle:	n/a
17	chr1:67600311-67600361	RPTEC	kidney:	n/a
18	chr1:67600229-67600279	HCT-116	colon:	n/a
19	chr1:67595214-67595264	U87	brain:	n/a
20	chr1:67600172-67600222	K562	blood:	n/a
21	chr1:67594788-67594838	HEK293	kidney:	embryo
22	chr1:67631342-67631392	HEK293	kidney:	embryo
23	chr1:67632028-67632078	Hepatocyte	liver:	n/a
24	chr1:67613819-67613869	HCT-116	colon:	n/a
25	chr1:67603174-67603224	SK-N-MC	brain:	n/a
26	chr1:67600428-67600478	HEEpiC	esophagus:	n/a
27	chr1:67603174-67603224	MCF-7	breast:	n/a
28	chr1:67600311-67600361	ovcar-3	ovarian:	n/a
29	chr1:67594274-67594324	HMEC	breast:	n/a
30	chr1:67594788-67594838	H1-hESC	embryonic stem cell:	embryo
31	chr1:67631342-67631392	AG04450	lung:	fetal
32	chr1:67600687-67600737	HCF	heart:	n/a
33	chr1:67632028-67632078	HEK293	kidney:	embryo
34	chr1:67600707-67600757	HRCEpiC	kidney:	n/a
35	chr1:67594788-67594838	NT2-D1	testis:	n/a
36	chr1:67632028-67632078	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:67600547-67600597	PFSK-1	brain:	n/a
38	chr1:67594274-67594324	HCT-116	colon:	n/a
39	chr1:67613911-67613961	CMK	blood:	n/a
40	chr1:67613911-67613961	MCF10A-Er-Src	breast:	n/a
41	chr1:67600311-67600361	SK-N-MC	brain:	n/a
42	chr1:67597928-67597978	HCPEpiC	choroid plexus:	n/a
43	chr1:67600687-67600737	HCM	heart:	n/a
44	chr1:67600229-67600279	GM19239	blood:	n/a
45	chr1:67631342-67631392	PrEC	prostate:	n/a
46	chr1:67594820-67594870	A549	lung:	n/a
47	chr1:67631214-67631264	HRE	kidney:	n/a
48	chr1:67600687-67600737	HMEC	breast:	n/a
49	chr1:67594788-67594838	GM19239	blood:	n/a
50	chr1:67600172-67600222	T-47D	breast:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:67596003..67598773-chr1:67600680..67602340,2	K562	blood:
2	chr1:67552378..67556698-chr1:67559401..67563184,5	K562	blood:
3	chr1:67561006..67563194-chr1:67569699..67571799,2	K562	blood:
4	chr1:67600516..67604047-chr1:67614399..67617708,3	K562	blood:
5	chr1:67461444..67462560-chr1:67614576..67615470,12	K562	blood:
6	chr1:67551344..67552961-chr1:67552970..67555808,2	K562	blood:
7	chr1:67561173..67563270-chr1:67569179..67571534,2	K562	blood:
8	chr1:67551656..67556031-chr1:67559263..67563184,6	K562	blood:
9	chr1:67582372..67583952-chr1:67586455..67588060,2	K562	blood:
10	chr1:67596003..67598773-chr1:67600680..67602340,2	K562	blood:
11	chr1:67635692..67638633-chr1:67640217..67642877,2	K562	blood:
12	chr1:67555800..67558037-chr1:67566353..67568285,2	K562	blood:
13	chr1:67461442..67462591-chr1:67614219..67615531,23	MCF-7	breast:
14	chr1:67582372..67583952-chr1:67586455..67588060,2	K562	blood:
15	chr1:67572936..67574606-chr1:67575289..67576798,2	K562	blood:
16	chr1:67511473..67513782-chr1:67612631..67614927,2	K562	blood:
17	chr1:67552378..67556698-chr1:67559401..67563184,5	K562	blood:
18	chr1:67558831..67564229-chr1:67565617..67569175,7	K562	blood:
19	chr1:67461406..67464362-chr1:67614424..67616124,2	K562	blood:
20	chr1:67461440..67462355-chr1:67614531..67615513,6	MCF-7	breast:
21	chr1:67564265..67566133-chr1:67568098..67570558,2	K562	blood:
22	chr1:67519541..67521560-chr1:67562573..67564185,2	K562	blood:
23	chr1:67637215..67639065-chr1:67640706..67643569,2	K562	blood:
24	chr1:67518927..67521401-chr1:67554492..67557377,2	K562	blood:
25	chr1:67561006..67563194-chr1:67569699..67571799,2	K562	blood:
26	chr1:67560393..67564229-chr1:67565692..67568839,3	K562	blood:
27	chr1:67555800..67558037-chr1:67566353..67568285,2	K562	blood:
28	chr1:67561173..67563270-chr1:67569179..67571534,2	K562	blood:
29	chr1:67230464..67231736-chr1:67614522..67615465,5	K562	blood:
30	chr1:67551656..67556031-chr1:67559263..67563184,6	K562	blood:
31	chr1:67637215..67639065-chr1:67640706..67643569,2	K562	blood:
32	chr1:67626230..67628264-chr1:67629535..67632198,2	K562	blood:
33	chr1:67610098..67611051-chr1:67676932..67677867,3	MCF-7	breast:
34	chr1:67635692..67638633-chr1:67640217..67642877,2	K562	blood:
35	chr1:67230851..67231401-chr1:67614599..67615362,2	MCF-7	breast:
36	chr1:67551344..67552961-chr1:67552970..67555808,2	K562	blood:
37	chr1:67591574..67593270-chr1:67608776..67611381,2	K562	blood:
38	chr1:67595628..67598773-chr1:67600680..67602546,3	K562	blood:
39	chr1:67631404..67633226-chr1:67635317..67637681,2	K562	blood:
40	chr1:67595628..67598773-chr1:67600680..67602546,3	K562	blood:
41	chr1:67572936..67574606-chr1:67575289..67576798,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1orf141-1	chr1:67596825-67596910	NONHSAT003771
2	lnc-C1orf141-1	chr1:67579297-67579439	NONHSAT003770
3	lnc-C1orf141-1	chr1:67600613-67600654	NONHSAT003770
4	lnc-C1orf141-1	chr1:67592849-67592940	NONHSAT003771
5	lnc-C1orf141-1	chr1:67557859-67559287	NONHSAT003770
6	lnc-C1orf141-1	chr1:67592849-67592940	NONHSAT003770
7	lnc-C1orf141-1	chr1:67568921-67569065	NONHSAT003770
8	lnc-C1orf141-1	chr1:67591435-67591592	NONHSAT003770
9	lnc-C1orf141-1	chr1:67600613-67600653	NONHSAT003771
10	lnc-C1orf141-1	chr1:67558078-67562004	NONHSAT003771
11	lnc-C1orf141-1	chr1:67577260-67577327	NONHSAT003770
12	lnc-C1orf141-1	chr1:67581035-67581147	NONHSAT003770
13	lnc-C1orf141-1	chr1:67561935-67562004	NONHSAT003770
14	lnc-C1orf141-1	chr1:67591435-67591592	NONHSAT003771
15	lnc-C1orf141-1	chr1:67596825-67596910	NONHSAT003770

No data

Variant related genes	Relation type
ENSG00000252433	TF binding region
IL23R	TF binding region
C1orf141	TF binding region
ENSG00000252433	CpG island
IL23R	CpG island
C1orf141	CpG island
ENSG00000252433	chromatin interactions
ENSG00000116704	chromatin interactions
ENSG00000203963	chromatin interactions
ENSG00000162594	chromatin interactions

Extended variants
information (count: 2875 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2875 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10789220	chr1:67551209-67551210	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs6663617	chr1:67551211-67551212	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs187962726	chr1:67551250-67551251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113323284	chr1:67551299-67551300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546804889	chr1:67551329-67551330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566695622	chr1:67551353-67551354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535746634	chr1:67551386-67551387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114877619	chr1:67551484-67551485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147997927	chr1:67551531-67551532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12078187	chr1:67551541-67551542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141673374	chr1:67551549-67551550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7552043	chr1:67551578-67551579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150543153	chr1:67551586-67551587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539508628	chr1:67551593-67551594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576364628	chr1:67551628-67551629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372997169	chr1:67551632-67551633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553228591	chr1:67551704-67551705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7552205	chr1:67551741-67551742	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs541586893	chr1:67551771-67551772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139567200	chr1:67551812-67551813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144453940	chr1:67551862-67551863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147420470	chr1:67551917-67551918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564104530	chr1:67551948-67551949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72676013	chr1:67551959-67551960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546641881	chr1:67551963-67551964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560320186	chr1:67551988-67551989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79809945	chr1:67552016-67552017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549457196	chr1:67552017-67552018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569513230	chr1:67552102-67552103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530460721	chr1:67552128-67552129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550613765	chr1:67552154-67552155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570436584	chr1:67552185-67552186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539542395	chr1:67552209-67552210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191911850	chr1:67552211-67552212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566713969	chr1:67552216-67552217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114665272	chr1:67552223-67552224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184472106	chr1:67552226-67552227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145331857	chr1:67552277-67552278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189170585	chr1:67552295-67552296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557733045	chr1:67552325-67552326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs12563964	chr1:67552377-67552378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577572867	chr1:67552414-67552415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs192419030	chr1:67552423-67552424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74912623	chr1:67552443-67552444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529490307	chr1:67552536-67552537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147663737	chr1:67552565-67552566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562907542	chr1:67552580-67552581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs550804325	chr1:67552618-67552619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs58274846	chr1:67552619-67552620	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs59805578	chr1:67552639-67552640	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	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
Melanoma	17363583	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
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:818 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67550600-67551800	Enhancers	Brain Inferior Temporal Lobe	brain
2	chr1:67551000-67551800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:67551200-67551400	Enhancers	Brain Angular Gyrus	brain
4	chr1:67551200-67551600	Enhancers	Brain Cingulate Gyrus	brain
5	chr1:67551200-67551600	Enhancers	Brain Hippocampus Middle	brain
6	chr1:67551200-67551600	Enhancers	Brain Substantia Nigra	brain
7	chr1:67551800-67552200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:67552000-67552400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr1:67552200-67552800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:67552200-67552800	Enhancers	HSMMtube	muscle
11	chr1:67552600-67553000	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr1:67552600-67555000	Enhancers	K562	blood
13	chr1:67554600-67555000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr1:67555000-67556400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr1:67555000-67563000	Weak transcription	K562	blood
16	chr1:67559800-67561400	Enhancers	HMEC	breast
17	chr1:67560000-67560800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr1:67560000-67561600	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr1:67560200-67561400	Enhancers	NHEK	skin
20	chr1:67560200-67562000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:67561000-67561200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:67561200-67561400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr1:67561200-67561400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr1:67561200-67561400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:67561200-67561600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:67561400-67562600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr1:67561400-67563000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:67561400-67563000	Weak transcription	HMEC	breast
29	chr1:67561600-67562600	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr1:67561600-67563000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr1:67561600-67563200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr1:67561600-67563800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:67562000-67562400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:67562400-67563600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr1:67562400-67563600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:67562600-67563400	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr1:67562600-67563600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr1:67562600-67563800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr1:67562600-67563800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr1:67562600-67563800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:67562600-67563800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:67562600-67563800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr1:67562600-67563800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr1:67562600-67563800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr1:67562800-67563600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr1:67563000-67563600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr1:67563000-67563600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:67563000-67563600	Enhancers	HMEC	breast
49	chr1:67563000-67563600	Enhancers	K562	blood
50	chr1:67563000-67563800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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