Variant report

Variant	esv3430321
Chromosome Location	chr8:57858417-58055129
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1583)
CpG islands
(count:1100)
Chromatin interactive
region (count:80)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1583 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:57885403-57885823	K562	blood:	n/a	n/a
2	ARID3A	chr8:57906339-57906829	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:58033807-58033945	K562	blood:	n/a	n/a
4	ARID3A	chr8:58026284-58026534	HepG2	liver:	n/a	n/a
5	ATF1	chr8:57885431-57885797	K562	blood:	n/a	n/a
6	ATF2	chr8:57912758-57913233	GM12878	blood:	n/a	n/a
7	ATF2	chr8:57912752-57913247	GM12878	blood:	n/a	n/a
8	BACH1	chr8:57905737-57905802	K562	blood:	n/a	n/a
9	BACH1	chr8:58049285-58049314	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:57905431-57905465	K562	blood:	n/a	n/a
11	BACH1	chr8:57905485-57907050	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr8:57912800-57913279	GM12878	blood:	n/a	chr8:57913095-57913105
13	BATF	chr8:57888344-57888598	GM12878	blood:	n/a	n/a
14	BATF	chr8:57912757-57913283	GM12878	blood:	n/a	chr8:57913095-57913105
15	BATF	chr8:57888386-57888590	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:57912856-57913205	GM12878	blood:	n/a	chr8:57913098-57913107 chr8:57913097-57913106
17	BCLAF1	chr8:57912806-57913232	GM12878	blood:	n/a	chr8:57913098-57913107 chr8:57913097-57913106
18	BHLHE40	chr8:57906370-57906418	K562	blood:	n/a	n/a
19	BHLHE40	chr8:57905294-57905811	K562	blood:	n/a	n/a
20	BHLHE40	chr8:57912981-57913162	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:57885416-57885772	K562	blood:	n/a	n/a
22	BHLHE40	chr8:57903793-57903822	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:57888243-57888601	GM12878	blood:	n/a	n/a
24	BRCA1	chr8:57905634-57905996	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr8:58026404-58026491	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr8:57905816-57905887	GM12878	blood:	n/a	n/a
27	CBX3	chr8:57954017-57954269	K562	blood:	n/a	n/a
28	CBX3	chr8:57866066-57866471	K562	blood:	n/a	n/a
29	CBX3	chr8:57863764-57863979	K562	blood:	n/a	n/a
30	CBX3	chr8:57863517-57863962	K562	blood:	n/a	n/a
31	CBX3	chr8:57866109-57866376	K562	blood:	n/a	n/a
32	CCNT2	chr8:57885455-57885918	K562	blood:	n/a	n/a
33	CCNT2	chr8:57905608-57906551	K562	blood:	n/a	chr8:57906265-57906274
34	CCNT2	chr8:57955891-57956181	K562	blood:	n/a	n/a
35	CCNT2	chr8:57879902-57880179	K562	blood:	n/a	chr8:57880092-57880112
36	CEBPB	chr8:57905589-57905789	K562	blood:	n/a	n/a
37	CEBPB	chr8:58021417-58021636	HepG2	liver:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
38	CEBPB	chr8:57882630-57882970	K562	blood:	n/a	chr8:57882808-57882819 chr8:57882808-57882821 chr8:57882809-57882820 chr8:57882810-57882819
39	CEBPB	chr8:57893519-57893708	HepG2	liver:	n/a	chr8:57893557-57893568
40	CEBPB	chr8:57978896-57979131	HepG2	liver:	n/a	chr8:57979043-57979054 chr8:57979044-57979055 chr8:57979045-57979054
41	CEBPB	chr8:58021346-58021751	HepG2	liver:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
42	CEBPB	chr8:57978888-57979179	A549	lung:	n/a	chr8:57979043-57979054 chr8:57979044-57979055 chr8:57979045-57979054
43	CEBPB	chr8:58021423-58021631	K562	blood:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
44	CEBPB	chr8:58021311-58021749	A549	lung:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
45	CEBPB	chr8:57966544-57966737	K562	blood:	n/a	chr8:57966649-57966662
46	CEBPB	chr8:58053895-58054196	IMR90	lung:	n/a	n/a
47	CEBPB	chr8:57973502-57973796	IMR90	lung:	n/a	chr8:57973559-57973572 chr8:57973677-57973688
48	CEBPB	chr8:58016949-58017131	HepG2	liver:	n/a	chr8:58017060-58017071
49	CEBPB	chr8:58053930-58054161	K562	blood:	n/a	n/a
50	CEBPB	chr8:58021361-58021734	A549	lung:	n/a	chr8:58021533-58021544 chr8:58021548-58021559

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:57909641-57909691	HIPEpiC	eye:	n/a
2	chr8:57906609-57906659	HAEpiC	amniotic membrane:	n/a
3	chr8:57909641-57909691	HIPEpiC	eye:	n/a
4	chr8:57906609-57906659	HAEpiC	amniotic membrane:	n/a
5	chr8:57905325-57905375	IMR90	lung:	fetal
6	chr8:57903300-57903350	HRCEpiC	kidney:	n/a
7	chr8:57909641-57909691	HepG2	liver:	n/a
8	chr8:58055024-58055074	HL-60	blood:	n/a
9	chr8:58053663-58053713	GM06990	blood:	n/a
10	chr8:57906837-57906887	K562	blood:	n/a
11	chr8:57907138-57907188	Jurkat	blood:	n/a
12	chr8:57907010-57907060	HUVEC	blood vessel:	n/a
13	chr8:57896881-57896931	RPTEC	kidney:	n/a
14	chr8:57903300-57903350	ovcar-3	ovarian:	n/a
15	chr8:57912015-57912065	IMR90	lung:	fetal
16	chr8:57905325-57905375	HCM	heart:	n/a
17	chr8:57906609-57906659	HMEC	breast:	n/a
18	chr8:57903300-57903350	PFSK-1	brain:	n/a
19	chr8:57903300-57903350	SK-N-SH_RA	brain:	n/a
20	chr8:57906363-57906413	Hela-S3	cervix:	n/a
21	chr8:57903300-57903350	LNCaP	prostate:	n/a
22	chr8:58055024-58055074	HRCEpiC	kidney:	n/a
23	chr8:57906363-57906413	GM12891	blood:	n/a
24	chr8:57907010-57907060	CMK	blood:	n/a
25	chr8:57905325-57905375	Hela-S3	cervix:	n/a
26	chr8:58054756-58054806	NHDF-neo	bronchial:	n/a
27	chr8:57906166-57906216	SK-N-SH_RA	brain:	n/a
28	chr8:57896881-57896931	HAEpiC	amniotic membrane:	n/a
29	chr8:57905325-57905375	MCF-7	breast:	n/a
30	chr8:57906543-57906593	MCF10A-Er-Src	breast:	n/a
31	chr8:57903300-57903350	HIPEpiC	eye:	n/a
32	chr8:57907138-57907188	NB4	blood:	n/a
33	chr8:57907138-57907188	CMK	blood:	n/a
34	chr8:57909641-57909691	U87	brain:	n/a
35	chr8:57905925-57905975	HNPCEpiC	eye:	n/a
36	chr8:57906609-57906659	Caco-2	colon:	n/a
37	chr8:57906058-57906108	HUVEC	blood vessel:	n/a
38	chr8:57912015-57912065	SK-N-MC	brain:	n/a
39	chr8:57906166-57906216	GM19239	blood:	n/a
40	chr8:58055024-58055074	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:57905325-57905375	K562	blood:	n/a
42	chr8:58055024-58055074	MCF-7	breast:	n/a
43	chr8:57906837-57906887	AG09309	skin:	n/a
44	chr8:57906609-57906659	SK-N-SH_RA	brain:	n/a
45	chr8:58055024-58055074	AG04449	skin:	fetal
46	chr8:57906609-57906659	AG04449	skin:	fetal
47	chr8:57906363-57906413	A549	lung:	n/a
48	chr8:58055024-58055074	Jurkat	blood:	n/a
49	chr8:57907010-57907060	HIPEpiC	eye:	n/a
50	chr8:58054756-58054806	AG04449	skin:	fetal

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:57892990..57895689-chr8:57900783..57903742,2	K562	blood:
2	chr8:57975894..57977879-chr8:57979464..57981694,2	K562	blood:
3	chr8:57942719..57945161-chr8:57946376..57948191,2	K562	blood:
4	chr8:57958323..57960463-chr8:57966619..57968564,2	MCF-7	breast:
5	chr8:57958323..57960463-chr8:57966619..57968564,2	MCF-7	breast:
6	chr8:57879369..57881990-chr8:57882038..57884592,4	K562	blood:
7	chr8:57905771..57907777-chr8:57914027..57916310,2	K562	blood:
8	chr8:57884164..57885822-chr8:57887000..57889844,2	K562	blood:
9	chr8:57883252..57884200-chr8:58025868..58026858,2	MCF-7	breast:
10	chr8:57869598..57872187-chr8:57872498..57874504,2	K562	blood:
11	chr8:57902387..57904313-chr8:58024035..58025722,2	K562	blood:
12	chr8:57905221..57907345-chr8:58041168..58043040,2	MCF-7	breast:
13	chr8:57879369..57881990-chr8:57882038..57884592,4	K562	blood:
14	chr8:57897319..57899698-chr8:57903198..57906434,3	K562	blood:
15	chr8:57883252..57884200-chr8:58025868..58026858,2	MCF-7	breast:
16	chr8:57897401..57901243-chr8:57902885..57906545,5	MCF-7	breast:
17	chr8:57943611..57945161-chr8:57946376..57947923,2	K562	blood:
18	chr8:57896099..57897893-chr8:57899981..57902361,2	K562	blood:
19	chr8:57891643..57894816-chr8:57903794..57907010,5	K562	blood:
20	chr8:57904732..57907333-chr8:57913016..57915349,2	MCF-7	breast:
21	chr8:57883335..57884050-chr8:58255790..58256539,2	K562	blood:
22	chr8:57871408..57873371-chr8:57876087..57877926,2	K562	blood:
23	chr8:57891643..57894816-chr8:57903794..57907010,5	K562	blood:
24	chr8:57879439..57881476-chr8:57883092..57885565,2	K562	blood:
25	chr8:57965882..57968408-chr8:57971486..57974461,2	K562	blood:
26	chr8:57975894..57977879-chr8:57979464..57981694,2	K562	blood:
27	chr8:57962948..57965572-chr8:57969601..57972127,2	K562	blood:
28	chr8:57942719..57945161-chr8:57946376..57948191,2	K562	blood:
29	chr8:57945103..57946884-chr8:57951548..57953264,2	K562	blood:
30	chr8:57886935..57888679-chr8:57892931..57895043,2	MCF-7	breast:
31	chr8:57891263..57893548-chr8:57905444..57907032,2	MCF-7	breast:
32	chr8:57966902..57969878-chr8:57971450..57973564,2	MCF-7	breast:
33	chr8:57883085..57884006-chr8:58025963..58027168,5	K562	blood:
34	chr8:57905480..57907391-chr8:57963038..57964617,2	MCF-7	breast:
35	chr8:57931933..57934764-chr8:57941798..57943983,2	K562	blood:
36	chr8:57921411..57924157-chr8:57925835..57928345,2	K562	blood:
37	chr8:57864003..57866464-chr8:57868673..57870578,2	MCF-7	breast:
38	chr8:58027851..58030791-chr8:58031054..58032684,2	K562	blood:
39	chr8:58027851..58030791-chr8:58031054..58032684,2	K562	blood:
40	chr8:57966902..57969878-chr8:57971450..57973564,2	MCF-7	breast:
41	chr8:57965882..57968408-chr8:57971486..57974461,2	K562	blood:
42	chr8:57869598..57872187-chr8:57872498..57874504,2	K562	blood:
43	chr8:58048196..58050433-chr8:58051015..58053775,2	K562	blood:
44	chr8:58048196..58050433-chr8:58051015..58053775,2	K562	blood:
45	chr8:57879439..57881476-chr8:57883092..57885565,2	K562	blood:
46	chr8:57864003..57866464-chr8:57868673..57870578,2	MCF-7	breast:
47	chr8:57969033..57971183-chr8:57975062..57976912,2	K562	blood:
48	chr8:57905771..57907695-chr8:57914637..57916310,2	K562	blood:
49	chr8:57969033..57971183-chr8:57975062..57976912,2	K562	blood:
50	chr8:57962948..57965572-chr8:57969601..57972127,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHCHD7-8	chr8:57864401-57864601	NONHSAT126721
2	lnc-CHCHD7-2	chr8:57942969-57942998	XLOC_006804
3	lnc-CHCHD7-2	chr8:57965315-57965702	XLOC_006804
4	lnc-CHCHD7-9	chr8:57868647-57868875	NONHSAT126722

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	IMPAD1	hsa-miR-155-5p	chr8:57870740-57870762

Variant related genes	Relation type
IMPAD1	TF binding region
ENSG00000197334	TF binding region
ENSG00000253301	TF binding region
RNA5SP266	TF binding region
IMPAD1	CpG island
ENSG00000197334	CpG island
ENSG00000253301	CpG island
RNA5SP266	CpG island
ENSG00000253871	chromatin interactions
ENSG00000104331	chromatin interactions

Extended variants
information (count: 5946 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5946 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568478559	chr8:57858449-57858450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs35204870	chr8:57858468-57858469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138435377	chr8:57858472-57858473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4738557	chr8:57858539-57858540	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs568195904	chr8:57858586-57858587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533978370	chr8:57858591-57858592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553826127	chr8:57858604-57858605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544780469	chr8:57858611-57858612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372663829	chr8:57858636-57858637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577211519	chr8:57858681-57858682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539705490	chr8:57858682-57858683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559009172	chr8:57858710-57858711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575683927	chr8:57858718-57858719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544410201	chr8:57858811-57858812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116195744	chr8:57858853-57858854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574974238	chr8:57858895-57858896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs56147332	chr8:57858898-57858899	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs560268400	chr8:57858942-57858943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532679871	chr8:57858958-57858959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184780637	chr8:57859020-57859021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs59335177	chr8:57859043-57859044	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs531321288	chr8:57859049-57859050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77522075	chr8:57859104-57859105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370466994	chr8:57859134-57859135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146355478	chr8:57859148-57859149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533603095	chr8:57859149-57859150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139715282	chr8:57859257-57859258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189193841	chr8:57859271-57859272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539768230	chr8:57859295-57859296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561575155	chr8:57859369-57859370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556477525	chr8:57859386-57859387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575586377	chr8:57859396-57859397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181832761	chr8:57859425-57859426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187092091	chr8:57859531-57859532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372905592	chr8:57859567-57859568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73681989	chr8:57859568-57859569	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs540329252	chr8:57859603-57859604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62511997	chr8:57859634-57859635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs561277728	chr8:57859648-57859649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577000669	chr8:57859667-57859668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189983049	chr8:57859706-57859707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562833134	chr8:57859709-57859710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs80129449	chr8:57859716-57859717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552417722	chr8:57859752-57859753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540314773	chr8:57859770-57859771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113983624	chr8:57859786-57859787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561483200	chr8:57859811-57859812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527394562	chr8:57859953-57859954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547489824	chr8:57859973-57859974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570690394	chr8:57859975-57859976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2028 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:57856200-57858800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:57856800-57858600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr8:57857200-57863200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr8:57858400-57858600	Enhancers	Brain Hippocampus Middle	brain
5	chr8:57858400-57858600	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr8:57858400-57858600	Enhancers	Brain Substantia Nigra	brain
7	chr8:57858600-57860600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr8:57858800-57859400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:57860800-57861000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr8:57862000-57862200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:57862800-57863600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr8:57863000-57866400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:57863200-57864000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:57863400-57874800	Weak transcription	Colon Smooth Muscle	Colon
15	chr8:57863600-57863800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
16	chr8:57863600-57864200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:57863600-57864200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
18	chr8:57863800-57866200	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr8:57863800-57878200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr8:57864200-57865200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:57865000-57866800	ZNF genes & repeats	Adipose Nuclei	Adipose
22	chr8:57865000-57866800	ZNF genes & repeats	HMEC	breast
23	chr8:57865200-57866600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr8:57865200-57866600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
25	chr8:57865200-57866800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:57865400-57866000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
27	chr8:57865400-57866800	ZNF genes & repeats	HSMM	muscle
28	chr8:57866000-57867800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:57866200-57866400	ZNF genes & repeats	Rectal Smooth Muscle	rectum
30	chr8:57866200-57866600	ZNF genes & repeats	Brain Hippocampus Middle	brain
31	chr8:57866200-57866600	ZNF genes & repeats	Fetal Lung	lung
32	chr8:57866200-57866600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
33	chr8:57866200-57867000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr8:57866400-57876200	Weak transcription	Rectal Smooth Muscle	rectum
35	chr8:57866400-57878600	Weak transcription	Ovary	ovary
36	chr8:57866400-57902600	Weak transcription	Pancreas	Pancrea
37	chr8:57866600-57870600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr8:57866600-57871000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr8:57866600-57872800	Weak transcription	Right Ventricle	heart
40	chr8:57866600-57874800	Weak transcription	Placenta	Placenta
41	chr8:57866600-57875400	Weak transcription	Fetal Lung	lung
42	chr8:57866600-57876000	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr8:57866600-57876400	Weak transcription	Brain Hippocampus Middle	brain
44	chr8:57866800-57868800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr8:57866800-57870800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:57866800-57870800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr8:57866800-57871000	Weak transcription	HMEC	breast
48	chr8:57866800-57872600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr8:57866800-57872600	Weak transcription	Adipose Nuclei	Adipose
50	chr8:57866800-57873200	Weak transcription	Primary T helper cells fromperipheralblood	blood

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