Variant report

Variant	esv3401841
Chromosome Location	chr8:86088225-86091073
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:706)
CpG islands
(count:551)
Chromatin interactive
region (count:15)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:706 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86089205-86089363	K562	blood:	n/a	n/a
2	ATF2	chr8:86089711-86090765	GM12878	blood:	n/a	n/a
3	ATF2	chr8:86089066-86089635	GM12878	blood:	n/a	n/a
4	ATF2	chr8:86088813-86089133	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:86089048-86089625	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:86089836-86090318	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:86089171-86089284	K562	blood:	n/a	n/a
8	BCLAF1	chr8:86089823-86090332	GM12878	blood:	n/a	chr8:86089940-86089949
9	BCLAF1	chr8:86088901-86090353	GM12878	blood:	n/a	chr8:86089457-86089466 chr8:86089592-86089605 chr8:86089331-86089344 chr8:86089346-86089355 chr8:86089940-86089949
10	BHLHE40	chr8:86089055-86089550	HepG2	liver:	n/a	n/a
11	BHLHE40	chr8:86089890-86090286	K562	blood:	n/a	chr8:86089902-86089918
12	BHLHE40	chr8:86088874-86089484	K562	blood:	n/a	n/a
13	BHLHE40	chr8:86089770-86090288	HepG2	liver:	n/a	chr8:86089902-86089918
14	BHLHE40	chr8:86089006-86090229	GM12878	blood:	n/a	chr8:86089902-86089918 chr8:86089584-86089600
15	BRCA1	chr8:86089947-86090399	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr8:86089793-86090370	K562	blood:	n/a	n/a
17	CBX3	chr8:86088854-86089428	K562	blood:	n/a	n/a
18	CBX3	chr8:86088903-86090404	HCT-116	colon:	n/a	n/a
19	CCNT2	chr8:86089167-86090285	K562	blood:	n/a	chr8:86089405-86089414 chr8:86089371-86089380
20	CEBPB	chr8:86089294-86089317	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:86089934-86090643	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr8:86089850-86089954	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPD	chr8:86089629-86090227	HepG2	liver:	n/a	n/a
24	CEBPD	chr8:86089717-86090003	HepG2	liver:	n/a	n/a
25	CHD1	chr8:86090280-86090549	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr8:86088834-86089581	H1-hESC	embryonic stem cell:	n/a	chr8:86089405-86089415
27	CHD1	chr8:86089749-86090681	GM12878	blood:	n/a	n/a
28	CHD1	chr8:86089910-86089988	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr8:86089033-86089596	H1-hESC	embryonic stem cell:	n/a	chr8:86089405-86089415
30	CHD2	chr8:86089057-86090292	Hela-S3	cervix:	n/a	chr8:86089405-86089415
31	CHD2	chr8:86089884-86090405	HepG2	liver:	n/a	n/a
32	CHD2	chr8:86089024-86090374	GM12878	blood:	n/a	chr8:86089405-86089415
33	CHD2	chr8:86089053-86089606	K562	blood:	n/a	chr8:86089405-86089415
34	CHD2	chr8:86089985-86090262	K562	blood:	n/a	n/a
35	CHD2	chr8:86089887-86090323	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr8:86089165-86089626	HepG2	liver:	n/a	chr8:86089405-86089415
37	CREB1	chr8:86089814-86090473	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr8:86089154-86089497	A549	lung:	n/a	n/a
39	CREB1	chr8:86089040-86089609	HepG2	liver:	n/a	n/a
40	CREB1	chr8:86089035-86089637	K562	blood:	n/a	n/a
41	CREB1	chr8:86089031-86089696	A549	lung:	n/a	n/a
42	CREB1	chr8:86089042-86090728	GM12878	blood:	n/a	n/a
43	CREB1	chr8:86089709-86090299	A549	lung:	n/a	n/a
44	CREB1	chr8:86089875-86090351	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr8:86089039-86089646	K562	blood:	n/a	n/a
46	CREB1	chr8:86089192-86089630	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr8:86089016-86090399	HepG2	liver:	n/a	n/a
48	CTBP2	chr8:86089276-86090700	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr8:86090087-86090273	Gliobla	brain:	n/a	n/a
50	CTCF	chr8:86089120-86089270	NHEK	skin:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86089106-86089156	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:86089333-86089383	RPTEC	kidney:	n/a
3	chr8:86089106-86089156	HPAEpiC	pulmonary alveolar:	n/a
4	chr8:86089333-86089383	RPTEC	kidney:	n/a
5	chr8:86090186-86090236	NHDF-neo	bronchial:	n/a
6	chr8:86089106-86089156	HRE	kidney:	n/a
7	chr8:86089500-86089550	U87	brain:	n/a
8	chr8:86090224-86090274	HAEpiC	amniotic membrane:	n/a
9	chr8:86089333-86089383	HEK293	kidney:	embryo
10	chr8:86089333-86089383	CMK	blood:	n/a
11	chr8:86089846-86089896	AG04449	skin:	fetal
12	chr8:86089106-86089156	K562	blood:	n/a
13	chr8:86090773-86090823	HEEpiC	esophagus:	n/a
14	chr8:86089333-86089383	ovcar-3	ovarian:	n/a
15	chr8:86089481-86089531	GM19239	blood:	n/a
16	chr8:86090224-86090274	GM12892	blood:	n/a
17	chr8:86089500-86089550	K562	blood:	n/a
18	chr8:86090773-86090823	HUVEC	blood vessel:	n/a
19	chr8:86090186-86090236	HEEpiC	esophagus:	n/a
20	chr8:86090186-86090236	CMK	blood:	n/a
21	chr8:86089333-86089383	AG09309	skin:	n/a
22	chr8:86089500-86089550	MCF-7	breast:	n/a
23	chr8:86089106-86089156	SAEC	small airway:	n/a
24	chr8:86089481-86089531	HPAEpiC	pulmonary alveolar:	n/a
25	chr8:86089333-86089383	U87	brain:	n/a
26	chr8:86090773-86090823	HNPCEpiC	eye:	n/a
27	chr8:86089333-86089383	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:86090224-86090274	HCPEpiC	choroid plexus:	n/a
29	chr8:86090773-86090823	Jurkat	blood:	n/a
30	chr8:86089333-86089383	HL-60	blood:	n/a
31	chr8:86089333-86089383	IMR90	lung:	fetal
32	chr8:86090224-86090274	HCT-116	colon:	n/a
33	chr8:86090186-86090236	HRPEpiC	eye:	n/a
34	chr8:86089500-86089550	SK-N-MC	brain:	n/a
35	chr8:86090773-86090823	GM12878	blood:	n/a
36	chr8:86089500-86089550	SK-N-SH	brain:	n/a
37	chr8:86090224-86090274	PANC-1	pancreas:	n/a
38	chr8:86089500-86089550	HNPCEpiC	eye:	n/a
39	chr8:86089481-86089531	AG09319	gingival:	n/a
40	chr8:86090186-86090236	T-47D	breast:	n/a
41	chr8:86090186-86090236	HIPEpiC	eye:	n/a
42	chr8:86089106-86089156	PANC-1	pancreas:	n/a
43	chr8:86089500-86089550	HRE	kidney:	n/a
44	chr8:86090773-86090823	HAEpiC	amniotic membrane:	n/a
45	chr8:86089333-86089383	Hela-S3	cervix:	n/a
46	chr8:86089106-86089156	HL-60	blood:	n/a
47	chr8:86090224-86090274	NH-A	brain:	n/a
48	chr8:86089481-86089531	SK-N-SH_RA	brain:	n/a
49	chr8:86089846-86089896	PrEC	prostate:	n/a
50	chr8:86089481-86089531	SK-N-MC	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:149899426..149900366-chr8:86089491..86090377,2	HCT-116	colon:
2	chr8:86088862..86093405-chr8:86093868..86100908,10	K562	blood:
3	chr8:86086312..86088635-chr8:86202652..86204401,2	MCF-7	breast:
4	chr8:86087523..86090287-chr8:86131220..86133061,4	K562	blood:
5	chr8:86088356..86092364-chr8:86131123..86134666,8	MCF-7	breast:
6	chr8:82753384..82754969-chr8:86089257..86091516,2	MCF-7	breast:
7	chr8:86088150..86092119-chr8:86130217..86134794,5	K562	blood:
8	chr8:86089298..86091951-chr8:86118252..86120782,3	MCF-7	breast:
9	chr8:86089844..86092252-chr8:86098327..86100668,2	MCF-7	breast:
10	chr8:86088170..86090782-chr8:86116952..86119231,3	MCF-7	breast:
11	chr8:86089162..86091404-chr8:86126321..86127950,2	MCF-7	breast:
12	chr8:86088315..86091850-chr8:86128947..86134706,9	MCF-7	breast:
13	chr21:17407538..17408042-chr8:86090577..86091119,2	MCF-7	breast:
14	chr8:86016436..86019868-chr8:86087554..86092567,7	K562	blood:
15	chr8:86088302..86092423-chr8:86099880..86105553,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf59-1	chr8:86089757-86090033	ENSG00000254208.1
2	lnc-C8orf59-1	chr8:86090195-86090385	ENSG00000254208.1
3	lnc-C8orf59-2	chr8:86089066-86089276	ENSG00000260493.1
4	lnc-C8orf59-2	chr8:86088034-86089297	ENSG00000260493.1

No data

Variant related genes	Relation type
ENSG00000254208	TF binding region
E2F5	TF binding region
ENSG00000260493	TF binding region
ENSG00000254208	CpG island
E2F5	CpG island
ENSG00000260493	CpG island
ENSG00000133739	chromatin interactions
ENSG00000176731	chromatin interactions
ENSG00000185015	chromatin interactions
ENSG00000252273	chromatin interactions
ENSG00000143368	chromatin interactions
ENSG00000104497	chromatin interactions
ENSG00000133740	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181956553	chr8:86088234-86088235	Weak transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
2	rs368769484	chr8:86088263-86088264	Weak transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs548041453	chr8:86088273-86088274	Weak transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs570516465	chr8:86088276-86088277	Weak transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs371456340	chr8:86088337-86088338	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
6	rs539489001	chr8:86088358-86088359	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
7	rs186079389	chr8:86088369-86088370	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
8	rs576155949	chr8:86088379-86088380	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
9	rs373736187	chr8:86088380-86088381	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs535927491	chr8:86088409-86088410	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs566471220	chr8:86088468-86088469	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
12	rs572176216	chr8:86088476-86088477	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
13	rs188978845	chr8:86088503-86088504	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
14	rs533498264	chr8:86088522-86088523	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
15	rs564329499	chr8:86088529-86088530	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
16	rs577993621	chr8:86088546-86088547	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
17	rs367553674	chr8:86088645-86088646	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
18	rs563253510	chr8:86088654-86088655	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
19	rs565967111	chr8:86088725-86088726	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
20	rs529015399	chr8:86088822-86088823	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
21	rs372083698	chr8:86088892-86088893	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
22	rs562167364	chr8:86088917-86088918	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs34730989	chr8:86088925-86088926	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
24	rs527839934	chr8:86088931-86088932	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs534870729	chr8:86088955-86088956	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs570857309	chr8:86088972-86088973	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
27	rs548909617	chr8:86089197-86089198	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs533424560	chr8:86089201-86089202	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs549796649	chr8:86089205-86089206	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
30	rs181678628	chr8:86089217-86089218	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs76828550	chr8:86089233-86089234	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
32	rs555781905	chr8:86089239-86089240	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs112015675	chr8:86089285-86089286	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
34	rs78400396	chr8:86089292-86089293	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
35	rs368610709	chr8:86089297-86089298	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
36	rs200760745	chr8:86089303-86089304	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs557983823	chr8:86089306-86089307	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs555264727	chr8:86089313-86089314	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs186745825	chr8:86089331-86089332	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs191533802	chr8:86089397-86089398	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs565561556	chr8:86089409-86089410	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs573553728	chr8:86089414-86089415	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs4150838	chr8:86089415-86089416	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs542361908	chr8:86089427-86089428	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs4150839	chr8:86089435-86089436	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs577731134	chr8:86089445-86089446	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs528169968	chr8:86089457-86089458	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs541255201	chr8:86089555-86089556	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs564323679	chr8:86089584-86089585	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs202019129	chr8:86089592-86089593	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	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
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
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86083600-86088600	Enhancers	Primary B cells from cord blood	blood
2	chr8:86084000-86088800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:86084600-86088600	Weak transcription	Thymus	Thymus
4	chr8:86084600-86088600	Weak transcription	K562	blood
5	chr8:86084600-86088800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr8:86084600-86088800	Weak transcription	Primary T cells from cord blood	blood
7	chr8:86084800-86088600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr8:86084800-86088600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr8:86084800-86088600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr8:86084800-86088800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:86084800-86088800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr8:86085200-86088800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr8:86085400-86088800	Weak transcription	Liver	Liver
14	chr8:86085600-86088800	Weak transcription	HepG2	liver
15	chr8:86086800-86088800	Enhancers	Primary hematopoietic stem cells	blood
16	chr8:86087000-86089000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr8:86087200-86088600	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr8:86087200-86088800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr8:86087200-86088800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr8:86087200-86088800	Enhancers	Fetal Thymus	thymus
21	chr8:86087400-86088800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:86087600-86088600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr8:86087600-86088800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr8:86087600-86089000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr8:86088000-86088400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr8:86088000-86088600	Enhancers	GM12878-XiMat	blood
27	chr8:86088000-86088800	Enhancers	Primary B cells from peripheral blood	blood
28	chr8:86088200-86088600	Enhancers	Dnd41	blood
29	chr8:86088200-86088600	Weak transcription	Hela-S3	cervix
30	chr8:86088200-86088800	Enhancers	Primary T cells fromperipheralblood	blood
31	chr8:86088200-86088800	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr8:86088200-86088800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr8:86088400-86088600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr8:86088400-86088800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr8:86088600-86088800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr8:86088600-86088800	Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr8:86088600-86088800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr8:86088600-86088800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr8:86088600-86088800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr8:86088600-86088800	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr8:86088600-86088800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr8:86088600-86088800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr8:86088600-86088800	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr8:86088600-86088800	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr8:86088600-86088800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:86088600-86088800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr8:86088600-86088800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr8:86088600-86088800	Enhancers	Brain Angular Gyrus	brain
49	chr8:86088600-86088800	Enhancers	Brain Hippocampus Middle	brain
50	chr8:86088600-86088800	Enhancers	Colon Smooth Muscle	Colon

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