Variant report

Variant	esv3406311
Chromosome Location	chr4:56580578-56840877
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3226)
CpG islands
(count:2813)
Chromatin interactive
region (count:166)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3226 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:56733160-56733642	K562	blood:	n/a	n/a
2	ARID3A	chr4:56602788-56603227	K562	blood:	n/a	n/a
3	ARID3A	chr4:56602821-56603153	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:56700241-56700501	K562	blood:	n/a	n/a
5	ARID3A	chr4:56707844-56707971	K562	blood:	n/a	n/a
6	ARID3A	chr4:56814765-56815291	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:56608965-56609070	K562	blood:	n/a	n/a
8	ARID3A	chr4:56814236-56814399	K562	blood:	n/a	n/a
9	ARID3A	chr4:56732295-56732942	K562	blood:	n/a	n/a
10	ARID3A	chr4:56719754-56719949	K562	blood:	n/a	n/a
11	ARID3A	chr4:56814620-56815710	K562	blood:	n/a	chr4:56815625-56815641
12	ARID3A	chr4:56815523-56816127	HepG2	liver:	n/a	chr4:56815625-56815641
13	ARID3A	chr4:56733156-56733529	HepG2	liver:	n/a	n/a
14	ARID3A	chr4:56602401-56602562	K562	blood:	n/a	n/a
15	ARID3A	chr4:56589584-56589800	K562	blood:	n/a	n/a
16	ARID3A	chr4:56719450-56719956	HepG2	liver:	n/a	n/a
17	ARID3A	chr4:56705383-56705392	K562	blood:	n/a	n/a
18	ARID3A	chr4:56599903-56600328	K562	blood:	n/a	n/a
19	ARID3A	chr4:56597276-56597725	K562	blood:	n/a	n/a
20	ARID3A	chr4:56595714-56597053	K562	blood:	n/a	n/a
21	ATF1	chr4:56732542-56732834	K562	blood:	n/a	n/a
22	ATF1	chr4:56719642-56719964	K562	blood:	n/a	n/a
23	ATF1	chr4:56595957-56597096	K562	blood:	n/a	n/a
24	ATF2	chr4:56813391-56813954	GM12878	blood:	n/a	n/a
25	ATF2	chr4:56813229-56814436	GM12878	blood:	n/a	n/a
26	ATF2	chr4:56814710-56815130	GM12878	blood:	n/a	n/a
27	ATF2	chr4:56719584-56720047	GM12878	blood:	n/a	n/a
28	ATF2	chr4:56685758-56686253	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr4:56733076-56733428	GM12878	blood:	n/a	n/a
30	ATF2	chr4:56814601-56815380	GM12878	blood:	n/a	n/a
31	ATF3	chr4:56719666-56719991	K562	blood:	n/a	n/a
32	ATF3	chr4:56732477-56732839	K562	blood:	n/a	n/a
33	ATF3	chr4:56599950-56600410	K562	blood:	n/a	n/a
34	ATF3	chr4:56700620-56700926	K562	blood:	n/a	n/a
35	ATF3	chr4:56600082-56600281	K562	blood:	n/a	n/a
36	ATF3	chr4:56719687-56720051	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF3	chr4:56634460-56634806	K562	blood:	n/a	n/a
38	ATF3	chr4:56719699-56719947	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF3	chr4:56719709-56719965	HepG2	liver:	n/a	n/a
40	ATF3	chr4:56719714-56719942	GM12878	blood:	n/a	n/a
41	ATF3	chr4:56719633-56720047	GM12878	blood:	n/a	n/a
42	BACH1	chr4:56608951-56609115	K562	blood:	n/a	n/a
43	BACH1	chr4:56814557-56815281	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr4:56688683-56688702	K562	blood:	n/a	n/a
45	BACH1	chr4:56722546-56722555	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr4:56751207-56751211	K562	blood:	n/a	n/a
47	BATF	chr4:56814755-56815080	GM12878	blood:	n/a	n/a
48	BATF	chr4:56814022-56814300	GM12878	blood:	n/a	n/a
49	BCLAF1	chr4:56813494-56814284	GM12878	blood:	n/a	n/a
50	BCLAF1	chr4:56814709-56815580	GM12878	blood:	n/a	chr4:56815020-56815033 chr4:56815289-56815302 chr4:56815251-56815264 chr4:56815101-56815110 chr4:56814922-56814935 chr4:56815325-56815338

(count:2813 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:56685972-56686022	GM12892	blood:	n/a
2	chr4:56720686-56720736	NHDF-neo	bronchial:	n/a
3	chr4:56660328-56660378	SK-N-SH	brain:	n/a
4	chr4:56812321-56812371	IMR90	lung:	fetal
5	chr4:56708175-56708225	HCT-116	colon:	n/a
6	chr4:56663994-56664044	NT2-D1	testis:	n/a
7	chr4:56719715-56719765	GM19239	blood:	n/a
8	chr4:56685972-56686022	GM12892	blood:	n/a
9	chr4:56720686-56720736	NHDF-neo	bronchial:	n/a
10	chr4:56660328-56660378	SK-N-SH	brain:	n/a
11	chr4:56812321-56812371	IMR90	lung:	fetal
12	chr4:56708175-56708225	HCT-116	colon:	n/a
13	chr4:56663994-56664044	NT2-D1	testis:	n/a
14	chr4:56719715-56719765	GM19239	blood:	n/a
15	chr4:56719908-56719958	U87	brain:	n/a
16	chr4:56660143-56660193	SAEC	small airway:	n/a
17	chr4:56659922-56659972	HCM	heart:	n/a
18	chr4:56818360-56818410	SK-N-SH	brain:	n/a
19	chr4:56660143-56660193	GM12892	blood:	n/a
20	chr4:56659985-56660035	GM19239	blood:	n/a
21	chr4:56659924-56659974	GM19239	blood:	n/a
22	chr4:56720686-56720736	BE2_C	brain:	n/a
23	chr4:56839901-56839951	NHDF-neo	bronchial:	n/a
24	chr4:56814934-56814984	K562	blood:	n/a
25	chr4:56659922-56659972	HRE	kidney:	n/a
26	chr4:56720227-56720277	HIPEpiC	eye:	n/a
27	chr4:56708175-56708225	BE2_C	brain:	n/a
28	chr4:56660460-56660510	GM19239	blood:	n/a
29	chr4:56719854-56719904	MCF-7	breast:	n/a
30	chr4:56660460-56660510	K562	blood:	n/a
31	chr4:56815070-56815120	HCM	heart:	n/a
32	chr4:56720227-56720277	HRPEpiC	eye:	n/a
33	chr4:56716944-56716994	Hela-S3	cervix:	n/a
34	chr4:56815263-56815313	NB4	blood:	n/a
35	chr4:56813860-56813910	CMK	blood:	n/a
36	chr4:56814925-56814975	PrEC	prostate:	n/a
37	chr4:56719908-56719958	H1-hESC	embryonic stem cell:	embryo
38	chr4:56685972-56686022	CMK	blood:	n/a
39	chr4:56815070-56815120	AG10803	skin:	n/a
40	chr4:56815070-56815120	Caco-2	colon:	n/a
41	chr4:56658357-56658407	RPTEC	kidney:	n/a
42	chr4:56719854-56719904	GM12892	blood:	n/a
43	chr4:56685972-56686022	NHBE	bronchial:	n/a
44	chr4:56659924-56659974	AG09319	gingival:	n/a
45	chr4:56719660-56719710	HMEC	breast:	n/a
46	chr4:56708175-56708225	AG04450	lung:	fetal
47	chr4:56815510-56815560	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:56660398-56660448	NH-A	brain:	n/a
49	chr4:56686245-56686295	NT2-D1	testis:	n/a
50	chr4:56815263-56815313	HNPCEpiC	eye:	n/a

(count:166 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:56637771..56639865-chr4:56697633..56699417,2	MCF-7	breast:
2	chr4:56812961..56814619-chr4:57166848..57168708,2	K562	blood:
3	chr4:56691986..56694448-chr4:56725201..56727859,2	K562	blood:
4	chr4:56600328..56605093-chr4:56606071..56610406,4	K562	blood:
5	chr4:56733409..56735263-chr4:56739400..56741094,2	MCF-7	breast:
6	chr4:56727071..56728991-chr4:56730888..56733080,2	K562	blood:
7	chr4:56758636..56761129-chr4:56795006..56797729,2	K562	blood:
8	chr4:56649556..56651202-chr4:56652557..56654365,2	K562	blood:
9	chr4:56719938..56721892-chr4:56731701..56734664,2	MCF-7	breast:
10	chr4:56587276..56591232-chr4:56591490..56593918,4	K562	blood:
11	chr4:56631566..56634040-chr4:56636504..56638538,3	K562	blood:
12	chr3:125313870..125314662-chr4:56814863..56815552,2	Hela-S3	cervix:
13	chr2:220118108..220118716-chr4:56719790..56720567,2	Hela-S3	cervix:
14	chr4:56718714..56721334-chr4:56789784..56792673,2	K562	blood:
15	chr4:56749468..56751302-chr4:56754110..56755765,2	K562	blood:
16	chr4:56747163..56749341-chr4:56759165..56761780,2	MCF-7	breast:
17	chr4:56807427..56809711-chr4:56812377..56814575,2	MCF-7	breast:
18	chr4:56705931..56707890-chr4:56715606..56717185,2	MCF-7	breast:
19	chr4:56794068..56796669-chr4:56814956..56816613,2	K562	blood:
20	chr4:56631564..56634040-chr4:56635751..56638538,2	K562	blood:
21	chr4:56777785..56781071-chr4:56783446..56787071,3	K562	blood:
22	chr4:56411840..56414684-chr4:56594475..56596628,2	MCF-7	breast:
23	chr4:56733409..56735263-chr4:56739400..56741094,2	MCF-7	breast:
24	chr4:56814876..56815558-chr6:30584657..30585422,2	Hela-S3	cervix:
25	chr4:56749468..56751302-chr4:56754110..56755765,2	K562	blood:
26	chr4:56756226..56757757-chr4:56764812..56767728,2	K562	blood:
27	chr4:56717920..56722163-chr4:56723001..56728347,7	K562	blood:
28	chr4:56310883..56311632-chr4:56601150..56602069,2	MCF-7	breast:
29	chr4:56632143..56634650-chr4:56645244..56648181,2	K562	blood:
30	chr4:56816608..56819327-chr4:56820355..56823340,3	K562	blood:
31	chr4:56685297..56688659-chr4:56689398..56693221,5	K562	blood:
32	chr4:56749868..56753196-chr4:56757101..56759826,3	K562	blood:
33	chr4:56770927..56772433-chr4:56774182..56776594,2	MCF-7	breast:
34	chr4:56813771..56816208-chr4:56822754..56824707,2	MCF-7	breast:
35	chr4:56695605..56697641-chr4:56707678..56709295,2	MCF-7	breast:
36	chr4:56649556..56651202-chr4:56652557..56654365,2	K562	blood:
37	chr4:56831199..56833182-chr4:56835848..56838788,2	K562	blood:
38	chr4:56632143..56634650-chr4:56645244..56648181,2	K562	blood:
39	chr4:56770927..56772433-chr4:56774182..56776594,2	MCF-7	breast:
40	chr4:56722903..56725254-chr4:56731032..56733800,2	K562	blood:
41	chr4:56310665..56311231-chr4:56732865..56733374,2	K562	blood:
42	chr4:56637771..56639865-chr4:56697633..56699417,2	MCF-7	breast:
43	chr4:56820475..56822078-chr4:56827472..56830252,2	MCF-7	breast:
44	chr4:56481534..56484408-chr4:56607415..56610057,2	K562	blood:
45	chr4:56411270..56413465-chr4:56811598..56813630,2	K562	blood:
46	chr4:56733117..56736188-chr4:56740397..56743875,4	K562	blood:
47	chr4:56581911..56585061-chr4:56585536..56588285,3	K562	blood:
48	chr4:56733117..56736188-chr4:56740397..56743875,4	K562	blood:
49	chr4:56411182..56412770-chr4:56812130..56814893,2	K562	blood:
50	chr4:56718974..56722726-chr4:56731263..56734718,5	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP135-2	chr4:56792992-56793318	NONHSAT096481
2	lnc-NMU-4	chr4:56831061-56831169	NONHSAT096488
3	lnc-NMU-4	chr4:56836939-56836996	NONHSAT096488
4	lnc-NMU-3	chr4:56814006-56814177	NONHSAT096484
5	lnc-NMU-3	chr4:56804560-56804569	NONHSAT096484
6	lnc-EXOC1-3	chr4:56828901-56829220	NONHSAT096487
7	lnc-NMU-3	chr4:56806683-56806798	NONHSAT096484
8	lnc-NMU-3	chr4:56814122-56815341	NONHSAT096485
9	lnc-CEP135-1	chr4:56794959-56795947	NONHSAT096482
10	lnc-NMU-4	chr4:56830360-56830521	NONHSAT096488
11	lnc-NMU-3	chr4:56804583-56805121	NONHSAT096484

No data

Variant related genes	Relation type
CEP135	TF binding region
ENSG00000222954	TF binding region
RNU6-276P	TF binding region
ENSG00000250821	TF binding region
RNU6-652P	TF binding region
EXOC1	TF binding region
CEP135	CpG island
ENSG00000222954	CpG island
RNU6-276P	CpG island
ENSG00000250821	CpG island
RNU6-652P	CpG island
EXOC1	CpG island
ENSG00000272969	chromatin interactions
ENSG00000090989	chromatin interactions
ENSG00000250821	chromatin interactions
ENSG00000202358	chromatin interactions
ENSG00000106603	chromatin interactions
ENSG00000144909	chromatin interactions
ENSG00000150712	chromatin interactions
ENSG00000174799	chromatin interactions
ENSG00000072849	chromatin interactions
ENSG00000105397	chromatin interactions
ENSG00000222954	chromatin interactions
ENSG00000269921	chromatin interactions
ENSG00000134851	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000249700	chromatin interactions
ENSG00000109255	chromatin interactions
ENSG00000128059	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000196584	chromatin interactions
ENSG00000157426	chromatin interactions
ENSG00000127824	chromatin interactions
ENSG00000167842	chromatin interactions
ENSG00000134852	chromatin interactions
ENSG00000128039	chromatin interactions
ENSG00000128050	chromatin interactions

Extended variants
information (count: 7284 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:7284 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368260528	chr4:56586429-56586430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532777210	chr4:56586470-56586471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532694461	chr4:56586511-56586512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146671783	chr4:56586574-56586575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188858062	chr4:56586605-56586606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537585155	chr4:56586634-56586635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140222219	chr4:56586635-56586636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567994179	chr4:56586652-56586653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551004006	chr4:56586787-56586788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533821431	chr4:56586850-56586851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73238305	chr4:56586890-56586891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs576598693	chr4:56586958-56586959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529740686	chr4:56586959-56586960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs193036210	chr4:56586973-56586974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558741546	chr4:56587023-56587024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs28654670	chr4:56587032-56587033	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs566610883	chr4:56587051-56587052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76433157	chr4:56587065-56587066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561312386	chr4:56587081-56587082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533866906	chr4:56587090-56587091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560896330	chr4:56587111-56587112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28622167	chr4:56587169-56587170	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs11721916	chr4:56587179-56587180	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs552797243	chr4:56587213-56587214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570562532	chr4:56587270-56587271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538011175	chr4:56587291-56587292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562987168	chr4:56587361-56587362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113138283	chr4:56587362-56587363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531413568	chr4:56587406-56587407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548014944	chr4:56587423-56587424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528324453	chr4:56587425-56587426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs56794069	chr4:56587566-56587567	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs574369911	chr4:56587576-56587577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377103334	chr4:56587625-56587626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144062250	chr4:56587634-56587635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570423535	chr4:56587675-56587676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs118008723	chr4:56587692-56587693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539388881	chr4:56587720-56587721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4386659	chr4:56587761-56587762	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs185099062	chr4:56587778-56587779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28670731	chr4:56587779-56587780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554779198	chr4:56587797-56587798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77122112	chr4:56587823-56587824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540643129	chr4:56587847-56587848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112743484	chr4:56587883-56587884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540334876	chr4:56587951-56587952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187474294	chr4:56588061-56588062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115500647	chr4:56588084-56588085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149046942	chr4:56588111-56588112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531828222	chr4:56588119-56588120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Autism	22543975	CNVD
Breast cancer	21785460	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4201 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56586400-56586600	Enhancers	K562	blood
2	chr4:56586600-56588400	Weak transcription	K562	blood
3	chr4:56588400-56589600	Enhancers	K562	blood
4	chr4:56589600-56590000	Flanking Active TSS	K562	blood
5	chr4:56590000-56590600	Enhancers	K562	blood
6	chr4:56590600-56591800	Weak transcription	K562	blood
7	chr4:56591800-56592400	Enhancers	K562	blood
8	chr4:56592400-56593400	Weak transcription	K562	blood
9	chr4:56593400-56595200	ZNF genes & repeats	K562	blood
10	chr4:56593800-56594000	Bivalent Enhancer	HSMMtube	muscle
11	chr4:56595000-56601200	Enhancers	Stomach Mucosa	stomach
12	chr4:56595200-56595600	Enhancers	K562	blood
13	chr4:56595600-56597600	Flanking Active TSS	K562	blood
14	chr4:56595800-56596400	Enhancers	Fetal Intestine Small	intestine
15	chr4:56595800-56596600	Enhancers	HMEC	breast
16	chr4:56596000-56597200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:56596400-56599600	Weak transcription	Fetal Intestine Small	intestine
18	chr4:56596600-56599200	Weak transcription	HMEC	breast
19	chr4:56597600-56598000	Enhancers	K562	blood
20	chr4:56598000-56598200	Flanking Active TSS	K562	blood
21	chr4:56598200-56599600	Enhancers	K562	blood
22	chr4:56599000-56600000	Enhancers	Fetal Intestine Large	intestine
23	chr4:56599200-56601000	Enhancers	HMEC	breast
24	chr4:56599600-56600400	Flanking Active TSS	K562	blood
25	chr4:56599600-56600600	Enhancers	Hela-S3	cervix
26	chr4:56599600-56600600	Enhancers	NHEK	skin
27	chr4:56599600-56600800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:56599600-56600800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:56599600-56601000	Enhancers	Fetal Intestine Small	intestine
30	chr4:56599800-56600600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:56600000-56600400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:56600000-56600400	Weak transcription	Fetal Intestine Large	intestine
33	chr4:56600000-56600400	Enhancers	A549	lung
34	chr4:56600200-56600400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:56600200-56600800	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr4:56600400-56601000	Enhancers	Fetal Intestine Large	intestine
37	chr4:56600400-56601000	Enhancers	K562	blood
38	chr4:56600600-56600800	Enhancers	Duodenum Mucosa	Duodenum
39	chr4:56600600-56601000	Enhancers	Colonic Mucosa	Colon
40	chr4:56600800-56602800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:56601000-56601400	Weak transcription	K562	blood
42	chr4:56601200-56602400	Weak transcription	Stomach Mucosa	stomach
43	chr4:56601400-56602800	Enhancers	K562	blood
44	chr4:56602400-56602600	Enhancers	Stomach Mucosa	stomach
45	chr4:56603000-56603200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr4:56608800-56609200	Enhancers	Hela-S3	cervix
47	chr4:56608800-56609200	Enhancers	HSMMtube	muscle
48	chr4:56608800-56609400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr4:56608800-56609400	Enhancers	Ovary	ovary
50	chr4:56608800-56609400	Enhancers	HMEC	breast

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