Variant report

Variant	esv1800867
Chromosome Location	chr8:58104763-58148292
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:930)
CpG islands
(count:2014)
Chromatin interactive
region (count:30)
LncRNA
region (count:41)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:930 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58122168-58122783	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:58137879-58138528	HepG2	liver:	n/a	n/a
3	ATF1	chr8:58122169-58123010	K562	blood:	n/a	n/a
4	ATF1	chr8:58142984-58143184	K562	blood:	n/a	n/a
5	ATF3	chr8:58137924-58138390	A549	lung:	n/a	n/a
6	BACH1	chr8:58122347-58122997	K562	blood:	n/a	n/a
7	BHLHE40	chr8:58118159-58118698	K562	blood:	n/a	n/a
8	BHLHE40	chr8:58105853-58106191	K562	blood:	n/a	n/a
9	BHLHE40	chr8:58137964-58138275	HepG2	liver:	n/a	n/a
10	BHLHE40	chr8:58127590-58127948	K562	blood:	n/a	n/a
11	BHLHE40	chr8:58122112-58123036	K562	blood:	n/a	n/a
12	BRCA1	chr8:58118301-58118654	GM12878	blood:	n/a	n/a
13	BRCA1	chr8:58127563-58127875	GM12878	blood:	n/a	n/a
14	BRCA1	chr8:58127438-58127751	HepG2	liver:	n/a	n/a
15	BRCA1	chr8:58122208-58123016	GM12878	blood:	n/a	n/a
16	BRCA1	chr8:58122170-58122971	HepG2	liver:	n/a	n/a
17	CBX3	chr8:58105849-58106177	K562	blood:	n/a	n/a
18	CCNT2	chr8:58105900-58106102	K562	blood:	n/a	n/a
19	CEBPB	chr8:58135455-58135719	HepG2	liver:	n/a	chr8:58135609-58135620
20	CEBPB	chr8:58137953-58138466	A549	lung:	n/a	n/a
21	CEBPB	chr8:58144842-58145071	A549	lung:	n/a	chr8:58144923-58144934
22	CEBPB	chr8:58122125-58123045	K562	blood:	n/a	n/a
23	CEBPB	chr8:58135497-58135726	HepG2	liver:	n/a	chr8:58135609-58135620
24	CEBPB	chr8:58135438-58135794	Hela-S3	cervix:	n/a	chr8:58135609-58135620
25	CEBPB	chr8:58135416-58135803	HepG2	liver:	n/a	chr8:58135609-58135620
26	CEBPB	chr8:58135434-58135802	A549	lung:	n/a	chr8:58135609-58135620
27	CEBPB	chr8:58135367-58135856	MCF-7	breast:	n/a	chr8:58135609-58135620
28	CEBPB	chr8:58138106-58138233	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:58135419-58135810	K562	blood:	n/a	chr8:58135609-58135620
30	CEBPB	chr8:58142920-58143205	A549	lung:	n/a	chr8:58143082-58143093
31	CEBPB	chr8:58142903-58143248	Hela-S3	cervix:	n/a	chr8:58143082-58143093
32	CEBPB	chr8:58135395-58135845	MCF-7	breast:	n/a	chr8:58135609-58135620
33	CEBPB	chr8:58144790-58145090	HepG2	liver:	n/a	chr8:58144923-58144934
34	CEBPB	chr8:58118292-58118614	HepG2	liver:	n/a	chr8:58118437-58118448
35	CEBPB	chr8:58142910-58143255	HepG2	liver:	n/a	chr8:58143082-58143093
36	CEBPB	chr8:58137871-58138537	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr8:58135434-58135730	K562	blood:	n/a	chr8:58135609-58135620
38	CEBPB	chr8:58144788-58145075	K562	blood:	n/a	chr8:58144923-58144934
39	CEBPB	chr8:58142924-58143273	IMR90	lung:	n/a	chr8:58143082-58143093
40	CEBPB	chr8:58118253-58118637	K562	blood:	n/a	chr8:58118437-58118448
41	CEBPB	chr8:58135407-58135877	A549	lung:	n/a	chr8:58135609-58135620
42	CEBPB	chr8:58138094-58138305	HepG2	liver:	n/a	n/a
43	CEBPB	chr8:58135426-58135823	K562	blood:	n/a	chr8:58135609-58135620
44	CEBPB	chr8:58138061-58138288	A549	lung:	n/a	n/a
45	CEBPB	chr8:58135428-58135788	IMR90	lung:	n/a	chr8:58135609-58135620
46	CEBPD	chr8:58135517-58135669	HepG2	liver:	n/a	n/a
47	CEBPZ	chr8:58118279-58118527	HepG2	liver:	n/a	n/a
48	CHD1	chr8:58118485-58118679	GM12878	blood:	n/a	n/a
49	CHD1	chr8:58122169-58123189	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr8:58127562-58127861	HepG2	liver:	n/a	n/a

(count:2014 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58138048-58138098	NH-A	brain:	n/a
2	chr8:58138048-58138098	NH-A	brain:	n/a
3	chr8:58132287-58132337	HIPEpiC	eye:	n/a
4	chr8:58122850-58122900	AoSMC	blood vessel:	n/a
5	chr8:58117541-58117591	AG10803	skin:	n/a
6	chr8:58128724-58128774	MCF-7	breast:	n/a
7	chr8:58122215-58122265	PrEC	prostate:	n/a
8	chr8:58128724-58128774	GM12878	blood:	n/a
9	chr8:58138048-58138098	NHDF-neo	bronchial:	n/a
10	chr8:58128466-58128516	AG09309	skin:	n/a
11	chr8:58106094-58106144	NHDF-neo	bronchial:	n/a
12	chr8:58121215-58121265	NHDF-neo	bronchial:	n/a
13	chr8:58123513-58123563	NT2-D1	testis:	n/a
14	chr8:58131602-58131652	ovcar-3	ovarian:	n/a
15	chr8:58117541-58117591	PFSK-1	brain:	n/a
16	chr8:58122215-58122265	SKMC	muscle:	n/a
17	chr8:58106520-58106570	AG04450	lung:	fetal
18	chr8:58123513-58123563	HCF	heart:	n/a
19	chr8:58122850-58122900	HAEpiC	amniotic membrane:	n/a
20	chr8:58128466-58128516	NH-A	brain:	n/a
21	chr8:58130041-58130091	SAEC	small airway:	n/a
22	chr8:58119141-58119191	Hela-S3	cervix:	n/a
23	chr8:58121215-58121265	HepG2	liver:	n/a
24	chr8:58131602-58131652	HCM	heart:	n/a
25	chr8:58120465-58120515	ProgFib	skin:	n/a
26	chr8:58117541-58117591	HRPEpiC	eye:	n/a
27	chr8:58121215-58121265	GM12891	blood:	n/a
28	chr8:58117541-58117591	LNCaP	prostate:	n/a
29	chr8:58122850-58122900	NB4	blood:	n/a
30	chr8:58106520-58106570	AoSMC	blood vessel:	n/a
31	chr8:58106598-58106648	NHDF-neo	bronchial:	n/a
32	chr8:58117541-58117591	HNPCEpiC	eye:	n/a
33	chr8:58129604-58129654	SAEC	small airway:	n/a
34	chr8:58118711-58118761	Jurkat	blood:	n/a
35	chr8:58119141-58119191	ovcar-3	ovarian:	n/a
36	chr8:58122215-58122265	CMK	blood:	n/a
37	chr8:58132446-58132496	GM12891	blood:	n/a
38	chr8:58122215-58122265	AG04450	lung:	fetal
39	chr8:58124249-58124299	HCF	heart:	n/a
40	chr8:58122850-58122900	NHDF-neo	bronchial:	n/a
41	chr8:58106598-58106648	BJ	skin:	n/a
42	chr8:58106520-58106570	BJ	skin:	n/a
43	chr8:58128466-58128516	GM12892	blood:	n/a
44	chr8:58106155-58106205	Hela-S3	cervix:	n/a
45	chr8:58118711-58118761	T-47D	breast:	n/a
46	chr8:58106094-58106144	GM19239	blood:	n/a
47	chr8:58122850-58122900	ProgFib	skin:	n/a
48	chr8:58132287-58132337	HRE	kidney:	n/a
49	chr8:58106094-58106144	HUVEC	blood vessel:	n/a
50	chr8:58106520-58106570	GM12878	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
2	chr8:58121826..58122902-chr8:58255580..58256503,3	MCF-7	breast:
3	chr8:58104914..58107604-chr8:58109994..58112221,3	K562	blood:
4	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
5	chr8:58134015..58136749-chr8:58138139..58140095,2	K562	blood:
6	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
7	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
8	chr8:58122191..58122786-chr8:58255142..58256110,2	K562	blood:
9	chr8:58145565..58148679-chr8:58153371..58155909,3	K562	blood:
10	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
11	chr8:58134015..58136749-chr8:58138139..58140095,2	K562	blood:
12	chr8:58137340..58139312-chr8:58141710..58144515,2	MCF-7	breast:
13	chr8:58143846..58145924-chr8:58146772..58148988,2	K562	blood:
14	chr8:58129429..58131931-chr8:58132415..58133992,2	K562	blood:
15	chr8:58145565..58149221-chr8:58153371..58158136,4	K562	blood:
16	chr8:58143846..58145924-chr8:58146772..58148988,2	K562	blood:
17	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
18	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
19	chr8:58135656..58136628-chr8:58255573..58256399,7	MCF-7	breast:
20	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
21	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
22	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
23	chr8:58094506..58095013-chr8:58135741..58136318,2	MCF-7	breast:
24	chr8:58137967..58139990-chr8:58271314..58273259,2	MCF-7	breast:
25	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
26	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
27	chr8:58137340..58139312-chr8:58141710..58144515,2	MCF-7	breast:
28	chr8:58129899..58132563-chr8:58137038..58139171,2	K562	blood:
29	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
30	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-8	chr8:58131615-58131697	ENSG00000253301.1
2	lnc-FAM110B-8	chr8:58120568-58120763	ENSG00000253301.1
3	lnc-FAM110B-8	chr8:58136443-58136530	NONHSAT126744
4	lnc-FAM110B-8	chr8:58131969-58132182	NONHSAT126741
5	lnc-FAM110B-8	chr8:58139050-58139184	NONHSAT126742
6	lnc-FAM110B-8	chr8:58131162-58131254	ENSG00000253301.1
7	lnc-FAM110B-8	chr8:58106149-58106248	ENSG00000253301.1
8	lnc-FAM110B-8	chr8:58131648-58131697	NONHSAT126741
9	lnc-FAM110B-8	chr8:58131938-58132182	ENSG00000253301.1
10	lnc-FAM110B-8	chr8:58130835-58130911	ENSG00000253301.1
11	lnc-FAM110B-8	chr8:58143951-58145195	ENSG00000253301.1
12	lnc-FAM110B-8	chr8:58133958-58134166	NONHSAT126741
13	lnc-FAM110B-8	chr8:58132670-58132854	ENSG00000253301.1
14	lnc-FAM110B-8	chr8:58142104-58142573	NONHSAT126742
15	lnc-FAM110B-8	chr8:58132670-58132854	NONHSAT126741
16	lnc-FAM110B-8	chr8:58131969-58132082	ENSG00000253301.1
17	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
18	lnc-FAM110B-8	chr8:58142104-58142287	ENSG00000253301.1
19	lnc-FAM110B-8	chr8:58142104-58142287	ENSG00000253301.1
20	lnc-FAM110B-8	chr8:58135154-58135255	NONHSAT126742
21	lnc-FAM110B-8	chr8:58131648-58131697	ENSG00000253301.1
22	lnc-FAM110B-8	chr8:58106179-58106275	ENSG00000253301.1
23	lnc-FAM110B-8	chr8:58135154-58135255	ENSG00000253301.1
24	lnc-FAM110B-8	chr8:58131969-58132126	ENSG00000253301.1
25	lnc-FAM110B-8	chr8:58134728-58134830	ENSG00000253301.1
26	lnc-FAM110B-8	chr8:58135154-58135255	NONHSAT126741
27	lnc-FAM110B-8	chr8:58132670-58132854	NONHSAT126742
28	lnc-FAM110B-8	chr8:58131969-58132182	ENSG00000253301.1
29	lnc-FAM110B-8	chr8:58142104-58142287	NONHSAT126741
30	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
31	lnc-FAM110B-8	chr8:58134728-58134830	NONHSAT126741
32	lnc-FAM110B-8	chr8:58132670-58132795	ENSG00000253301.1
33	lnc-FAM110B-8	chr8:58131093-58131254	ENSG00000253301.1
34	lnc-FAM110B-8	chr8:58135154-58135255	ENSG00000253301.1
35	lnc-FAM110B-8	chr8:58143951-58145388	NONHSAT126741
36	lnc-FAM110B-8	chr8:58131885-58132182	NONHSAT126742
37	lnc-FAM110B-8	chr8:58133958-58134166	ENSG00000253301.1
38	lnc-FAM110B-8	chr8:58133148-58133297	ENSG00000253301.1
39	lnc-FAM110B-8	chr8:58142009-58146182	NONHSAT126744
40	lnc-FAM110B-8	chr8:58121058-58121191	ENSG00000253301.1
41	lnc-FAM110B-8	chr8:58132670-58132854	ENSG00000253301.1

No data

Variant related genes	Relation type
ENSG00000253301	TF binding region
ENSG00000251142	TF binding region
ENSG00000253301	CpG island
ENSG00000251142	CpG island
ENSG00000253871	chromatin interactions
ENSG00000253301	chromatin interactions

Extended variants
information (count: 2374 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2374 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560467571	chr8:58105403-58105404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532296317	chr8:58105404-58105405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552444331	chr8:58105422-58105423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565372933	chr8:58105604-58105605	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs189821082	chr8:58105605-58105606	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs17194529	chr8:58105647-58105648	Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs142751797	chr8:58105716-58105717	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs66477547	chr8:58105763-58105764	Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs375741838	chr8:58105767-58105768	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs566827670	chr8:58105778-58105779	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs182147706	chr8:58105781-58105782	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs558919617	chr8:58105784-58105785	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs75644437	chr8:58105793-58105794	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs371059090	chr8:58105795-58105796	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs537514371	chr8:58105797-58105798	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs574321511	chr8:58105814-58105815	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs386725758	chr8:58105856-58105857	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs56066782	chr8:58105857-58105858	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs17802743	chr8:58105897-58105898	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs375832982	chr8:58105908-58105909	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs564968880	chr8:58105926-58105927	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs528529809	chr8:58105927-58105928	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs577247221	chr8:58105944-58105945	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs55955962	chr8:58105952-58105953	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs397933649	chr8:58105953-58105954	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs16921807	chr8:58105967-58105968	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs372853258	chr8:58105993-58105994	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs56235637	chr8:58106008-58106009	Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs117008184	chr8:58106023-58106024	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs77494377	chr8:58106030-58106031	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs529991664	chr8:58106036-58106037	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs16921808	chr8:58106049-58106050	Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs566815342	chr8:58106051-58106052	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs532694050	chr8:58106056-58106057	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs16921810	chr8:58106067-58106068	Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs569316350	chr8:58106070-58106071	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs567034099	chr8:58106071-58106072	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs538441625	chr8:58106095-58106096	Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs532874963	chr8:58106111-58106112	Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs554318611	chr8:58106114-58106115	Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs568206283	chr8:58106118-58106119	Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs533758045	chr8:58106141-58106142	Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs372984165	chr8:58106152-58106153	Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs375583280	chr8:58106167-58106168	Enhancers Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs577191318	chr8:58106174-58106175	Enhancers Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs545753492	chr8:58106182-58106183	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs556439516	chr8:58106193-58106194	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs13253625	chr8:58106206-58106207	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs16920056	chr8:58106218-58106219	Weak transcription Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs373501573	chr8:58106230-58106231	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58105400-58105600	Enhancers	K562	blood
2	chr8:58105600-58106000	Flanking Active TSS	K562	blood
3	chr8:58105800-58106000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:58106000-58106200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:58106000-58107200	Active TSS	K562	blood
6	chr8:58106200-58114800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:58111800-58112200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr8:58114800-58115400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:58115400-58118200	Weak transcription	Right Atrium	heart
10	chr8:58116000-58117400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:58116200-58117000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:58116200-58117200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:58116400-58117000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
16	chr8:58116400-58117200	ZNF genes & repeats	Spleen	Spleen
17	chr8:58116400-58117400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr8:58116400-58118000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr8:58116600-58116800	ZNF genes & repeats	Brain Hippocampus Middle	brain
20	chr8:58116600-58117000	Enhancers	Gastric	stomach
21	chr8:58116600-58117200	ZNF genes & repeats	Fetal Kidney	kidney
22	chr8:58116600-58117200	ZNF genes & repeats	Pancreas	Pancrea
23	chr8:58116600-58117600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:58116600-58118800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr8:58116800-58118200	Weak transcription	Brain Hippocampus Middle	brain
26	chr8:58117000-58118200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:58117000-58118200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:58117000-58118200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr8:58117000-58118200	Weak transcription	Gastric	stomach
30	chr8:58117000-58119000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr8:58117200-58118200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:58117200-58118200	Weak transcription	Fetal Kidney	kidney
33	chr8:58117400-58118200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:58117800-58118800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
35	chr8:58118000-58118800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
36	chr8:58118000-58118800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr8:58118000-58118800	ZNF genes & repeats	Brain Germinal Matrix	brain
38	chr8:58118000-58118800	ZNF genes & repeats	Pancreas	Pancrea
39	chr8:58118200-58118400	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
40	chr8:58118200-58118600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
41	chr8:58118200-58118600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
42	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Large	intestine
43	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Small	intestine
44	chr8:58118200-58118600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
45	chr8:58118200-58118600	ZNF genes & repeats	Placenta	Placenta
46	chr8:58118200-58118600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
47	chr8:58118200-58118600	ZNF genes & repeats	NHEK	skin
48	chr8:58118200-58118800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
49	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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