Variant report

Variant	nsv1017564
Chromosome Location	chr8:61577791-61617812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1319)
CpG islands
(count:1160)
Chromatin interactive
region (count:81)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1319 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:61600764-61600889	K562	blood:	n/a	n/a
2	ARID3A	chr8:61593545-61594034	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:61602262-61602471	K562	blood:	n/a	n/a
4	ARID3A	chr8:61596742-61597109	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:61590920-61591120	HepG2	liver:	n/a	n/a
6	ATF1	chr8:61602255-61602614	K562	blood:	n/a	n/a
7	ATF2	chr8:61596444-61597137	GM12878	blood:	n/a	n/a
8	ATF2	chr8:61615294-61616309	GM12878	blood:	n/a	n/a
9	BACH1	chr8:61592278-61592518	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:61591471-61591593	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:61590482-61590769	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr8:61615723-61616061	GM12878	blood:	n/a	n/a
13	BATF	chr8:61615776-61616101	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:61588907-61589211	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCLAF1	chr8:61615788-61616501	GM12878	blood:	n/a	chr8:61616012-61616021 chr8:61615973-61615982 chr8:61616058-61616067
16	BCLAF1	chr8:61590647-61591239	GM12878	blood:	n/a	chr8:61590872-61590881 chr8:61591105-61591114 chr8:61590987-61591000
17	BCLAF1	chr8:61590827-61591194	GM12878	blood:	n/a	chr8:61590872-61590881 chr8:61591105-61591114 chr8:61590987-61591000
18	BHLHE40	chr8:61590963-61591612	GM12878	blood:	n/a	chr8:61590997-61591013 chr8:61591549-61591565 chr8:61590992-61591008
19	BHLHE40	chr8:61591969-61592133	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:61615073-61616131	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:61606952-61607152	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:61591945-61592141	K562	blood:	n/a	n/a
23	BHLHE40	chr8:61602476-61602513	K562	blood:	n/a	n/a
24	BHLHE40	chr8:61591029-61591114	K562	blood:	n/a	n/a
25	BHLHE40	chr8:61585322-61585381	K562	blood:	n/a	n/a
26	BRCA1	chr8:61591024-61591101	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr8:61616355-61616374	GM12878	blood:	n/a	n/a
28	BRCA1	chr8:61591591-61591640	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr8:61592639-61592724	H1-hESC	embryonic stem cell:	n/a	n/a
30	CBX3	chr8:61588541-61588947	K562	blood:	n/a	n/a
31	CCNT2	chr8:61602304-61602594	K562	blood:	n/a	n/a
32	CCNT2	chr8:61590709-61593275	K562	blood:	n/a	chr8:61592658-61592667 chr8:61592537-61592546
33	CEBPB	chr8:61593762-61594078	HepG2	liver:	n/a	chr8:61593899-61593908 chr8:61593897-61593908
34	CEBPB	chr8:61591030-61591201	K562	blood:	n/a	n/a
35	CEBPB	chr8:61593560-61594094	Hela-S3	cervix:	n/a	chr8:61593899-61593908 chr8:61593897-61593908
36	CEBPB	chr8:61593737-61594064	HepG2	liver:	n/a	chr8:61593899-61593908 chr8:61593897-61593908
37	CEBPB	chr8:61608986-61609170	K562	blood:	n/a	n/a
38	CEBPB	chr8:61593705-61594101	A549	lung:	n/a	chr8:61593899-61593908 chr8:61593897-61593908
39	CEBPB	chr8:61582547-61582820	K562	blood:	n/a	n/a
40	CEBPB	chr8:61590398-61591278	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr8:61591022-61591278	IMR90	lung:	n/a	n/a
42	CEBPB	chr8:61593713-61594098	K562	blood:	n/a	chr8:61593899-61593908 chr8:61593897-61593908
43	CEBPB	chr8:61593716-61594081	HepG2	liver:	n/a	chr8:61593899-61593908 chr8:61593897-61593908
44	CEBPB	chr8:61590998-61591209	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:61582553-61582816	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr8:61593733-61594071	MCF-7	breast:	n/a	chr8:61593899-61593908 chr8:61593897-61593908
47	CEBPB	chr8:61593697-61594061	K562	blood:	n/a	chr8:61593899-61593908 chr8:61593897-61593908
48	CEBPB	chr8:61591028-61591229	A549	lung:	n/a	n/a
49	CEBPB	chr8:61593769-61593979	HepG2	liver:	n/a	chr8:61593899-61593908 chr8:61593897-61593908
50	CEBPB	chr8:61593610-61594101	H1-hESC	embryonic stem cell:	n/a	chr8:61593899-61593908 chr8:61593897-61593908

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:61590588-61590638	HNPCEpiC	eye:	n/a
2	chr8:61590588-61590638	HNPCEpiC	eye:	n/a
3	chr8:61613721-61613771	HNPCEpiC	eye:	n/a
4	chr8:61596860-61596910	SK-N-MC	brain:	n/a
5	chr8:61591199-61591249	SKMC	muscle:	n/a
6	chr8:61590787-61590837	SKMC	muscle:	n/a
7	chr8:61593696-61593746	HCF	heart:	n/a
8	chr8:61596860-61596910	NB4	blood:	n/a
9	chr8:61591199-61591249	HRPEpiC	eye:	n/a
10	chr8:61593040-61593090	HAEpiC	amniotic membrane:	n/a
11	chr8:61591199-61591249	PFSK-1	brain:	n/a
12	chr8:61593696-61593746	LNCaP	prostate:	n/a
13	chr8:61591461-61591511	NB4	blood:	n/a
14	chr8:61591461-61591511	AG10803	skin:	n/a
15	chr8:61591199-61591249	U87	brain:	n/a
16	chr8:61591199-61591249	T-47D	breast:	n/a
17	chr8:61591436-61591486	MCF10A-Er-Src	breast:	n/a
18	chr8:61591939-61591989	NB4	blood:	n/a
19	chr8:61592088-61592138	Hela-S3	cervix:	n/a
20	chr8:61591939-61591989	PFSK-1	brain:	n/a
21	chr8:61613721-61613771	ECC-1	luminal epithelium:	n/a
22	chr8:61592088-61592138	SK-N-MC	brain:	n/a
23	chr8:61591436-61591486	HUVEC	blood vessel:	n/a
24	chr8:61592727-61592777	Caco-2	colon:	n/a
25	chr8:61591436-61591486	Hepatocyte	liver:	n/a
26	chr8:61590588-61590638	T-47D	breast:	n/a
27	chr8:61606295-61606345	Hela-S3	cervix:	n/a
28	chr8:61596860-61596910	AG09309	skin:	n/a
29	chr8:61588587-61588637	GM19239	blood:	n/a
30	chr8:61606295-61606345	NT2-D1	testis:	n/a
31	chr8:61592088-61592138	AG04449	skin:	fetal
32	chr8:61592727-61592777	HRCEpiC	kidney:	n/a
33	chr8:61613721-61613771	PFSK-1	brain:	n/a
34	chr8:61590718-61590768	GM12878	blood:	n/a
35	chr8:61591939-61591989	HIPEpiC	eye:	n/a
36	chr8:61596860-61596910	AG10803	skin:	n/a
37	chr8:61592088-61592138	ProgFib	skin:	n/a
38	chr8:61592088-61592138	SAEC	small airway:	n/a
39	chr8:61591436-61591486	SK-N-SH_RA	brain:	n/a
40	chr8:61590787-61590837	K562	blood:	n/a
41	chr8:61593040-61593090	AG10803	skin:	n/a
42	chr8:61591939-61591989	GM06990	blood:	n/a
43	chr8:61606295-61606345	BJ	skin:	n/a
44	chr8:61591398-61591448	HEEpiC	esophagus:	n/a
45	chr8:61592727-61592777	NH-A	brain:	n/a
46	chr8:61606295-61606345	GM12892	blood:	n/a
47	chr8:61590718-61590768	HRCEpiC	kidney:	n/a
48	chr8:61591204-61591254	SK-N-SH	brain:	n/a
49	chr8:61590718-61590768	MCF-7	breast:	n/a
50	chr8:61613721-61613771	HRCEpiC	kidney:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:61610380..61613389-chr8:61616371..61618193,3	MCF-7	breast:
2	chr8:61600702..61602522-chr8:61602539..61605188,2	K562	blood:
3	chr8:61604857..61607132-chr8:61609872..61611507,2	MCF-7	breast:
4	chr8:61590644..61591624-chrX:119737473..119738364,2	Hela-S3	cervix:
5	chr8:61599708..61602124-chr8:61603749..61606422,3	MCF-7	breast:
6	chr11:72463368..72463911-chr8:61592033..61592792,2	Hela-S3	cervix:
7	chr8:61601943..61604368-chr8:61616321..61619419,3	K562	blood:
8	chr8:61594274..61596445-chr8:61605915..61607443,2	MCF-7	breast:
9	chr8:61604857..61607132-chr8:61609872..61611507,2	MCF-7	breast:
10	chr8:61428381..61431496-chr8:61588452..61591900,3	K562	blood:
11	chr8:61599531..61602030-chr8:61683939..61686653,2	MCF-7	breast:
12	chr8:61596105..61598331-chr8:61606151..61608898,3	MCF-7	breast:
13	chr8:61612691..61616083-chr8:61619050..61621954,3	K562	blood:
14	chr8:61586135..61588890-chr8:61597344..61600255,2	MCF-7	breast:
15	chr8:61563979..61567563-chr8:61575798..61578846,3	MCF-7	breast:
16	chr8:61571219..61575228-chr8:61591571..61593615,3	MCF-7	breast:
17	chr8:61599708..61602124-chr8:61603749..61606422,3	MCF-7	breast:
18	chr8:61599554..61605342-chr8:61607995..61613853,8	K562	blood:
19	chr8:61597723..61599279-chr8:61608776..61610801,2	K562	blood:
20	chr8:61592791..61594650-chr8:61754871..61757414,2	K562	blood:
21	chr8:61596105..61598331-chr8:61606151..61608898,3	MCF-7	breast:
22	chr8:61595844..61597847-chr8:61600108..61602179,3	MCF-7	breast:
23	chr8:61602668..61604287-chr8:61616194..61618289,2	MCF-7	breast:
24	chr8:61614401..61615964-chr8:61617449..61618958,2	MCF-7	breast:
25	chr8:61564632..61566993-chr8:61599888..61601960,2	MCF-7	breast:
26	chr8:61564072..61567835-chr8:61581660..61584768,3	MCF-7	breast:
27	chr8:61595542..61601111-chr8:61606456..61610511,8	K562	blood:
28	chr8:61605995..61607571-chr8:61609134..61612024,2	MCF-7	breast:
29	chr8:59570989..59573111-chr8:61592746..61594650,2	MCF-7	breast:
30	chr8:61595659..61597988-chr8:61649091..61651205,2	MCF-7	breast:
31	chr8:61601943..61604368-chr8:61616321..61619419,3	K562	blood:
32	chr16:20911706..20912684-chr8:61590659..61591241,2	Hela-S3	cervix:
33	chr8:61563298..61566288-chr8:61597428..61599462,2	K562	blood:
34	chr8:61603796..61605326-chr8:61626958..61629344,2	MCF-7	breast:
35	chr8:61582013..61586353-chr8:61586778..61592648,6	K562	blood:
36	chr8:61563005..61568398-chr8:61588453..61593214,14	K562	blood:
37	chr8:61564434..61565085-chr8:61591483..61592116,2	Hela-S3	cervix:
38	chr8:61577127..61579062-chr8:61640050..61642549,2	MCF-7	breast:
39	chr8:61595542..61601111-chr8:61606456..61610511,8	K562	blood:
40	chr8:61558670..61560650-chr8:61587707..61590411,2	K562	blood:
41	chr8:61569858..61572736-chr8:61576944..61578909,2	K562	blood:
42	chr8:61562679..61568216-chr8:61588453..61593754,19	K562	blood:
43	chr8:61594133..61596295-chr8:61945003..61948640,3	K562	blood:
44	chr8:61579081..61581848-chr8:61589057..61591546,3	K562	blood:
45	chr8:61592636..61594603-chr8:61965419..61967444,2	MCF-7	breast:
46	chr8:61559343..61568621-chr8:61588061..61597189,35	MCF-7	breast:
47	chr8:61601737..61603348-chr8:61606675..61608350,2	MCF-7	breast:
48	chr8:61571937..61573571-chr8:61588900..61590755,2	MCF-7	breast:
49	chr8:61605995..61607571-chr8:61609134..61612024,2	MCF-7	breast:
50	chr8:61536123..61537975-chr8:61580798..61583756,2	K562	blood:

No data

Variant related genes	Relation type
CHD7	TF binding region
CHD7	CpG island
ENSG00000188215	chromatin interactions
ENSG00000234171	chromatin interactions
ENSG00000254869	chromatin interactions
ENSG00000171316	chromatin interactions
ENSG00000035681	chromatin interactions
ENSG00000255289	chromatin interactions
ENSG00000142178	chromatin interactions
ENSG00000104388	chromatin interactions
ENSG00000232119	chromatin interactions
ENSG00000186635	chromatin interactions
ENSG00000102897	chromatin interactions
ENSG00000171865	chromatin interactions
ENSG00000251396	chromatin interactions

Extended variants
information (count: 1440 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1440 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142512825	chr8:61577825-61577826	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs73685654	chr8:61577827-61577828	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs192763976	chr8:61577842-61577843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs185280265	chr8:61577845-61577846	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs546235426	chr8:61577851-61577852	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs542309335	chr8:61577852-61577853	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs79956284	chr8:61577907-61577908	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142474068	chr8:61577912-61577913	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564701055	chr8:61577923-61577924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562026146	chr8:61577951-61577952	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556091011	chr8:61577960-61577961	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540532949	chr8:61578021-61578022	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs190160478	chr8:61578061-61578062	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs192144685	chr8:61578115-61578116	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544380875	chr8:61578121-61578122	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532292573	chr8:61578127-61578128	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs115505259	chr8:61578137-61578138	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs184588033	chr8:61578203-61578204	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547270242	chr8:61578204-61578205	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs368848149	chr8:61578212-61578213	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs114494407	chr8:61578250-61578251	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs375541766	chr8:61578269-61578270	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs151323187	chr8:61578273-61578274	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs550429676	chr8:61578297-61578298	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs546624078	chr8:61578334-61578335	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs72650439	chr8:61578407-61578408	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs140469501	chr8:61578444-61578445	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557159170	chr8:61578446-61578447	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs569396555	chr8:61578518-61578519	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539895707	chr8:61578545-61578546	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558143242	chr8:61578595-61578596	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573198970	chr8:61578761-61578762	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs540621617	chr8:61578794-61578795	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555817140	chr8:61578845-61578846	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs180774811	chr8:61579095-61579096	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs186058562	chr8:61579153-61579154	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373056706	chr8:61579172-61579173	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs533015581	chr8:61579183-61579184	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138331229	chr8:61579197-61579198	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs605701	chr8:61579213-61579214	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs371653442	chr8:61579214-61579215	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566937317	chr8:61579263-61579264	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533976369	chr8:61579277-61579278	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs552828106	chr8:61579292-61579293	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560475568	chr8:61579325-61579326	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573995412	chr8:61579340-61579341	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs659805	chr8:61579356-61579357	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs141281749	chr8:61579359-61579360	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373356561	chr8:61579384-61579385	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545560862	chr8:61579396-61579397	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
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
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1381 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61584200-61585200	Enhancers	Fetal Brain Male	brain
2	chr8:61584400-61585200	Enhancers	Fetal Brain Female	brain
3	chr8:61584600-61584800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr8:61585600-61586400	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr8:61586000-61586400	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr8:61586400-61590400	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr8:61586400-61590400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr8:61588200-61588600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
9	chr8:61588200-61589200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
10	chr8:61588400-61588600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
11	chr8:61588400-61588600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
12	chr8:61588400-61588600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
13	chr8:61588400-61588800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
14	chr8:61588400-61589400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
15	chr8:61588400-61589400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr8:61588400-61590400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
17	chr8:61588600-61588800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
18	chr8:61588600-61588800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
19	chr8:61588600-61588800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
20	chr8:61588600-61588800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:61588600-61589000	Enhancers	H9 Cell Line	embryonic stem cell
22	chr8:61588600-61589000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
23	chr8:61588800-61589200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
24	chr8:61588800-61589200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
25	chr8:61588800-61590400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
26	chr8:61589000-61589200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
27	chr8:61589000-61589200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:61589200-61589400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
29	chr8:61589200-61589400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
30	chr8:61589200-61589400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
31	chr8:61589200-61589400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
32	chr8:61589200-61589400	Enhancers	HMEC	breast
33	chr8:61589200-61590000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:61589200-61590200	Enhancers	NHEK	skin
35	chr8:61589400-61589600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr8:61589400-61590200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
37	chr8:61589400-61590200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
38	chr8:61589400-61590400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
39	chr8:61589400-61590600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr8:61589600-61590000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr8:61589600-61590400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr8:61589600-61590600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr8:61590000-61590200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:61590000-61590200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
45	chr8:61590000-61590200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:61590000-61590400	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr8:61590000-61590400	Enhancers	Adipose Nuclei	Adipose
48	chr8:61590000-61590400	Enhancers	A549	lung
49	chr8:61590000-61590800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:61590000-61593600	Active TSS	Rectal Mucosa Donor 29	rectum

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