Variant report

Variant	nsv916392
Chromosome Location	chr8:50827638-51395140
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1960)
CpG islands
(count:1040)
Chromatin interactive
region (count:38)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1960 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:51351100-51351279	HepG2	liver:	n/a	n/a
2	ATF1	chr8:51210088-51210191	K562	blood:	n/a	n/a
3	ATF2	chr8:50968957-50969420	GM12878	blood:	n/a	n/a
4	ATF2	chr8:50969058-50969384	GM12878	blood:	n/a	n/a
5	ATF3	chr8:51310791-51311060	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr8:51310845-51311121	K562	blood:	n/a	n/a
7	ATF3	chr8:51310742-51311085	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:50867988-50868444	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:51380375-51380444	K562	blood:	n/a	n/a
10	BACH1	chr8:51204453-51204562	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:51322783-51322854	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:51360829-51360868	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:50867209-50867386	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:50892249-50892339	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr8:51057978-51058142	GM12878	blood:	n/a	n/a
16	BATF	chr8:50969021-50969265	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:50969028-50969333	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:50969022-50969362	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:51038532-51038842	GM12878	blood:	n/a	chr8:51038771-51038792
20	BHLHE40	chr8:51310826-51311066	K562	blood:	n/a	n/a
21	BHLHE40	chr8:51310789-51311051	HepG2	liver:	n/a	n/a
22	BHLHE40	chr8:50969028-50969399	GM12878	blood:	n/a	n/a
23	BRCA1	chr8:50873303-50873331	HepG2	liver:	n/a	n/a
24	BRCA1	chr8:51310893-51310975	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr8:50999011-50999073	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr8:50968793-50969924	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr8:50886853-50887178	A549	lung:	n/a	chr8:50887017-50887028
28	CEBPB	chr8:50844206-50844462	MCF-7	breast:	n/a	chr8:50844305-50844316
29	CEBPB	chr8:50844116-50844485	Hela-S3	cervix:	n/a	chr8:50844305-50844316
30	CEBPB	chr8:50892506-50892785	A549	lung:	n/a	chr8:50892652-50892663
31	CEBPB	chr8:50855601-50855816	HepG2	liver:	n/a	chr8:50855669-50855680
32	CEBPB	chr8:51320425-51320659	HepG2	liver:	n/a	chr8:51320549-51320560
33	CEBPB	chr8:51212610-51212958	IMR90	lung:	n/a	n/a
34	CEBPB	chr8:51212701-51212837	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr8:51295153-51295450	A549	lung:	n/a	chr8:51295254-51295263 chr8:51295252-51295263 chr8:51295254-51295265
36	CEBPB	chr8:50898826-50899188	IMR90	lung:	n/a	chr8:50899007-50899018 chr8:50899008-50899017 chr8:50899006-50899019 chr8:50899006-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899008-50899017 chr8:50899006-50899019
37	CEBPB	chr8:50941263-50941546	IMR90	lung:	n/a	chr8:50941381-50941392
38	CEBPB	chr8:51153154-51153293	H1-hESC	embryonic stem cell:	n/a	chr8:51153238-51153251
39	CEBPB	chr8:51013698-51013774	A549	lung:	n/a	n/a
40	CEBPB	chr8:51167350-51167687	MCF-7	breast:	n/a	chr8:51167453-51167470
41	CEBPB	chr8:50941250-50941558	HepG2	liver:	n/a	chr8:50941381-50941392
42	CEBPB	chr8:51176175-51176483	IMR90	lung:	n/a	chr8:51176300-51176311
43	CEBPB	chr8:50980388-50980486	K562	blood:	n/a	n/a
44	CEBPB	chr8:50997569-50997735	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:51184339-51184584	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr8:50946736-50947055	HepG2	liver:	n/a	chr8:50946882-50946893
47	CEBPB	chr8:50952403-50952800	Hela-S3	cervix:	n/a	chr8:50952625-50952636 chr8:50952624-50952641 chr8:50952625-50952638
48	CEBPB	chr8:51310770-51311151	H1-hESC	embryonic stem cell:	n/a	chr8:51310953-51310964
49	CEBPB	chr8:50879850-50880092	MCF-7	breast:	n/a	n/a
50	CEBPB	chr8:51052112-51052647	Hela-S3	cervix:	n/a	chr8:51052494-51052505

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:50892893-50892943	HEK293	kidney:	embryo
2	chr8:51039471-51039521	CMK	blood:	n/a
3	chr8:51199947-51199997	MCF10A-Er-Src	breast:	n/a
4	chr8:50892893-50892943	HEK293	kidney:	embryo
5	chr8:51039471-51039521	CMK	blood:	n/a
6	chr8:51199947-51199997	MCF10A-Er-Src	breast:	n/a
7	chr8:50968578-50968628	LNCaP	prostate:	n/a
8	chr8:50847816-50847866	ovcar-3	ovarian:	n/a
9	chr8:50891767-50891817	HCT-116	colon:	n/a
10	chr8:51039471-51039521	HCPEpiC	choroid plexus:	n/a
11	chr8:50891767-50891817	Jurkat	blood:	n/a
12	chr8:51039471-51039521	ECC-1	luminal epithelium:	n/a
13	chr8:50875600-50875650	PANC-1	pancreas:	n/a
14	chr8:50947399-50947449	HEK293	kidney:	embryo
15	chr8:50904638-50904688	GM12891	blood:	n/a
16	chr8:50875600-50875650	SKMC	muscle:	n/a
17	chr8:50980859-50980909	SK-N-SH	brain:	n/a
18	chr8:50980859-50980909	SK-N-SH_RA	brain:	n/a
19	chr8:51095593-51095643	SK-N-SH_RA	brain:	n/a
20	chr8:50904638-50904688	U87	brain:	n/a
21	chr8:50980859-50980909	NT2-D1	testis:	n/a
22	chr8:50847816-50847866	K562	blood:	n/a
23	chr8:50891767-50891817	SK-N-SH_RA	brain:	n/a
24	chr8:51288552-51288602	IMR90	lung:	fetal
25	chr8:50847816-50847866	HCM	heart:	n/a
26	chr8:51199947-51199997	T-47D	breast:	n/a
27	chr8:50837079-50837129	HRE	kidney:	n/a
28	chr8:50947399-50947449	SK-N-SH	brain:	n/a
29	chr8:51364244-51364294	HRPEpiC	eye:	n/a
30	chr8:51199947-51199997	HCF	heart:	n/a
31	chr8:50947399-50947449	NH-A	brain:	n/a
32	chr8:51039471-51039521	Hela-S3	cervix:	n/a
33	chr8:51364244-51364294	SK-N-SH	brain:	n/a
34	chr8:50891864-50891914	IMR90	lung:	fetal
35	chr8:51364244-51364294	NB4	blood:	n/a
36	chr8:50968578-50968628	GM19239	blood:	n/a
37	chr8:50968578-50968628	ProgFib	skin:	n/a
38	chr8:50947399-50947449	BE2_C	brain:	n/a
39	chr8:50968578-50968628	PANC-1	pancreas:	n/a
40	chr8:50968578-50968628	IMR90	lung:	fetal
41	chr8:51095593-51095643	H1-hESC	embryonic stem cell:	embryo
42	chr8:51364244-51364294	HEK293	kidney:	embryo
43	chr8:50847816-50847866	HMEC	breast:	n/a
44	chr8:51095593-51095643	HUVEC	blood vessel:	n/a
45	chr8:50892893-50892943	ovcar-3	ovarian:	n/a
46	chr8:51288552-51288602	K562	blood:	n/a
47	chr8:50980859-50980909	U87	brain:	n/a
48	chr8:50891864-50891914	HNPCEpiC	eye:	n/a
49	chr8:50892702-50892752	H1-hESC	embryonic stem cell:	embryo
50	chr8:50904638-50904688	HRE	kidney:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:51030711..51032424-chr8:51036929..51039858,2	MCF-7	breast:
2	chr8:50753724..50754320-chr8:51310816..51311345,2	MCF-7	breast:
3	chr1:144893909..144894771-chr8:51229590..51230343,2	MCF-7	breast:
4	chr8:51194558..51197541-chr8:51202196..51204695,2	MCF-7	breast:
5	chr8:51219065..51222213-chr8:51225649..51228332,3	K562	blood:
6	chr8:50832548..50835126-chr8:50839783..50841421,2	K562	blood:
7	chr8:50947077..50947745-chr8:51310573..51311162,2	MCF-7	breast:
8	chr8:50861606..50863840-chr8:50871624..50874600,2	MCF-7	breast:
9	chr8:50858643..50860623-chr8:50860794..50862890,2	K562	blood:
10	chr13:32746778..32747333-chr8:51314361..51315226,2	MCF-7	breast:
11	chr8:50925829..50927969-chr8:50932438..50935189,2	MCF-7	breast:
12	chr8:51187159..51189399-chr8:51189828..51191872,2	MCF-7	breast:
13	chr8:51050537..51053146-chr8:51056966..51059260,2	K562	blood:
14	chr8:49891255..49891972-chr8:51310445..51311051,2	MCF-7	breast:
15	chr8:50947077..50947745-chr8:51310573..51311162,2	MCF-7	breast:
16	chr8:50861606..50863840-chr8:50871624..50874600,2	MCF-7	breast:
17	chr8:51252100..51253925-chr8:51256216..51258662,2	MCF-7	breast:
18	chr8:50709168..50710848-chr8:50931158..50933465,2	MCF-7	breast:
19	chr8:51187159..51189399-chr8:51189828..51191872,2	MCF-7	breast:
20	chr8:50988839..50990732-chr8:50993883..50996257,2	K562	blood:
21	chr8:51252100..51253925-chr8:51256216..51258662,2	MCF-7	breast:
22	chr8:51194558..51197541-chr8:51202196..51204695,2	MCF-7	breast:
23	chr8:51372315..51374214-chr8:51375832..51377998,2	K562	blood:
24	chr8:50858643..50860623-chr8:50860794..50862890,2	K562	blood:
25	chr8:50826287..50827033-chr8:51310198..51311230,3	MCF-7	breast:
26	chr8:50906818..50909515-chr8:50916418..50918690,2	K562	blood:
27	chr8:50988839..50990732-chr8:50993883..50996257,2	K562	blood:
28	chr8:50947214..50948091-chr8:51310516..51311364,3	MCF-7	breast:
29	chr8:50851071..50853810-chr8:50856546..50858320,2	MCF-7	breast:
30	chr8:51219065..51222213-chr8:51225649..51228332,3	K562	blood:
31	chr8:50906818..50909515-chr8:50916418..50918690,2	K562	blood:
32	chr8:50851071..50853810-chr8:50856546..50858320,2	MCF-7	breast:
33	chr8:50947214..50948091-chr8:51310516..51311364,3	MCF-7	breast:
34	chr8:50832548..50835126-chr8:50839783..50841421,2	K562	blood:
35	chr8:51050537..51053146-chr8:51056966..51059260,2	K562	blood:
36	chr8:51372315..51374214-chr8:51375832..51377998,2	K562	blood:
37	chr8:51030711..51032424-chr8:51036929..51039858,2	MCF-7	breast:
38	chr8:50925829..50927969-chr8:50932438..50935189,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf22-15	chr8:51085121-51085195	NONHSAT126524
2	lnc-C8orf22-6	chr8:51294466-51294835	ENSG00000253849.1
3	lnc-C8orf22-15	chr8:51199098-51199413	NONHSAT126524
4	lnc-C8orf22-14	chr8:51076059-51076529	NONHSAT126523
5	lnc-C8orf22-6	chr8:51293575-51293638	ENSG00000253849.1

No data

Variant related genes	Relation type
ENSG00000253849	TF binding region
SNTG1	TF binding region
ENSG00000253849	CpG island
SNTG1	CpG island

Extended variants
information (count: 17770 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:17770 , 50 per page) page: 1 2 3 4 5 6 7 ... 356

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549769017	chr8:50827702-50827703	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs139576260	chr8:50827726-50827727	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs149711213	chr8:50827735-50827736	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs146756600	chr8:50827748-50827749	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs191217557	chr8:50827773-50827774	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs563349778	chr8:50827776-50827777	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs114487119	chr8:50827831-50827832	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs557656153	chr8:50827834-50827835	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs573819522	chr8:50827863-50827864	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs182961701	chr8:50827974-50827975	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs1486258	chr8:50827976-50827977	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs527674683	chr8:50827980-50827981	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs552192010	chr8:50827992-50827993	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs2450290	chr8:50828008-50828009	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs188301139	chr8:50828049-50828050	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs561517072	chr8:50828081-50828082	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs568657464	chr8:50828100-50828101	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs535736346	chr8:50828126-50828127	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs192815989	chr8:50828129-50828130	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs566423949	chr8:50828150-50828151	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs539432916	chr8:50828214-50828215	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs371197613	chr8:50828231-50828232	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs557820578	chr8:50828247-50828248	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs375452842	chr8:50828266-50828267	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs376321341	chr8:50828269-50828270	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs370713540	chr8:50828270-50828271	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs78066771	chr8:50828279-50828280	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs542130145	chr8:50828301-50828302	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs540915177	chr8:50828304-50828305	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs68134005	chr8:50828356-50828357	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs183117628	chr8:50828362-50828363	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs187765573	chr8:50828365-50828366	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs545768142	chr8:50828374-50828375	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs564157983	chr8:50828381-50828382	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs2450289	chr8:50828426-50828427	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs192476283	chr8:50828441-50828442	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140372312	chr8:50828477-50828478	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529489801	chr8:50828480-50828481	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563616166	chr8:50828497-50828498	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185015917	chr8:50828528-50828529	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533695740	chr8:50828532-50828533	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551361253	chr8:50828558-50828559	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575393842	chr8:50828657-50828658	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140771222	chr8:50828736-50828737	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs55714316	chr8:50828739-50828740	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs397688578	chr8:50828745-50828746	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370887956	chr8:50828746-50828747	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200289794	chr8:50828748-50828749	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201529689	chr8:50828749-50828750	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs202130327	chr8:50828750-50828751	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	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
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	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
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD
Type 1 diabetes	21085585	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
22q11 deletion syndrome	20357662	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:50821600-50829000	Active TSS	Brain Germinal Matrix	brain
2	chr8:50821800-50827800	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr8:50821800-50828600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:50822000-50828400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:50823400-50828400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr8:50824000-50828600	Active TSS	Brain Anterior Caudate	brain
7	chr8:50824600-50831600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr8:50824800-50830000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:50825000-50831800	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr8:50826200-50828600	Active TSS	Fetal Brain Female	brain
11	chr8:50826600-50830000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr8:50826800-50829800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr8:50826800-50830000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr8:50826800-50830000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr8:50827000-50828400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr8:50827200-50829800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr8:50827200-50829800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr8:50827600-50828200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr8:50827600-50829600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr8:50827800-50828000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
21	chr8:50828000-50828200	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr8:50828200-50828800	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr8:50828200-50829800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr8:50828200-50833800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr8:50828400-50830000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr8:50828600-50831200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr8:50828600-50836000	Weak transcription	Fetal Brain Female	brain
28	chr8:50828800-50834200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr8:50829000-50829800	Weak transcription	Brain Germinal Matrix	brain
30	chr8:50829600-50830000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr8:50829800-50830200	Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr8:50829800-50830200	Enhancers	Brain Germinal Matrix	brain
33	chr8:50829800-50830600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr8:50829800-50830800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr8:50829800-50832000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr8:50829800-50833400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr8:50830000-50830400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:50830000-50830400	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr8:50830000-50830400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr8:50830000-50830600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr8:50830000-50830800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr8:50830000-50833600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr8:50830200-50830600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr8:50830200-50834800	Weak transcription	Brain Germinal Matrix	brain
45	chr8:50830400-50831200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr8:50830600-50831000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr8:50830600-50833200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr8:50830600-50833400	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr8:50830800-50831200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr8:50831000-50832400	Enhancers	HUES6 Cell Line	embryonic stem cell

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