Variant report

Variant	esv2757281
Chromosome Location	chr8:91090821-91235335
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1239)
CpG islands
(count:854)
Chromatin interactive
region (count:177)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1239 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:91209454-91210582	K562	blood:	n/a	n/a
2	ARID3A	chr8:91181970-91182158	K562	blood:	n/a	n/a
3	ARID3A	chr8:91199734-91200847	K562	blood:	n/a	n/a
4	ARID3A	chr8:91151183-91151514	K562	blood:	n/a	n/a
5	ARID3A	chr8:91201265-91201605	K562	blood:	n/a	n/a
6	ARID3A	chr8:91207321-91209160	K562	blood:	n/a	n/a
7	ARID3A	chr8:91233441-91235765	K562	blood:	n/a	chr8:91234374-91234390 chr8:91234375-91234391
8	ARID3A	chr8:91189858-91190228	K562	blood:	n/a	n/a
9	ARID3A	chr8:91177637-91178012	K562	blood:	n/a	n/a
10	ARID3A	chr8:91206455-91206706	K562	blood:	n/a	n/a
11	ARID3A	chr8:91131335-91131588	K562	blood:	n/a	n/a
12	ARID3A	chr8:91131371-91131596	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:91197575-91197607	K562	blood:	n/a	n/a
14	ARID3A	chr8:91179832-91181174	K562	blood:	n/a	chr8:91180698-91180714
15	ARID3A	chr8:91232553-91232869	K562	blood:	n/a	n/a
16	ARID3A	chr8:91177147-91177182	HepG2	liver:	n/a	n/a
17	ARID3A	chr8:91226852-91227587	K562	blood:	n/a	chr8:91227468-91227484 chr8:91227469-91227485
18	ATF1	chr8:91233514-91234151	K562	blood:	n/a	n/a
19	ATF1	chr8:91206488-91206711	K562	blood:	n/a	n/a
20	ATF1	chr8:91177393-91178071	K562	blood:	n/a	n/a
21	ATF1	chr8:91179800-91180610	K562	blood:	n/a	n/a
22	ATF1	chr8:91181881-91182239	K562	blood:	n/a	n/a
23	ATF1	chr8:91209606-91210003	K562	blood:	n/a	n/a
24	ATF1	chr8:91199917-91200320	K562	blood:	n/a	n/a
25	ATF2	chr8:91094721-91095187	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr8:91094837-91095401	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr8:91209573-91209933	K562	blood:	n/a	n/a
28	ATF3	chr8:91199828-91200380	K562	blood:	n/a	n/a
29	ATF3	chr8:91179801-91180574	K562	blood:	n/a	n/a
30	BACH1	chr8:91145605-91145882	K562	blood:	n/a	n/a
31	BACH1	chr8:91180264-91180616	K562	blood:	n/a	n/a
32	BACH1	chr8:91094845-91095154	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr8:91210982-91211099	K562	blood:	n/a	n/a
34	BACH1	chr8:91234438-91234544	K562	blood:	n/a	n/a
35	BACH1	chr8:91095350-91095470	K562	blood:	n/a	n/a
36	BACH1	chr8:91194972-91195225	K562	blood:	n/a	n/a
37	BACH1	chr8:91178587-91178653	K562	blood:	n/a	n/a
38	BACH1	chr8:91209681-91209874	K562	blood:	n/a	n/a
39	BACH1	chr8:91223178-91223353	K562	blood:	n/a	n/a
40	BCL3	chr8:91199768-91200282	K562	blood:	n/a	chr8:91200101-91200110 chr8:91200100-91200109
41	BCLAF1	chr8:91199822-91200353	K562	blood:	n/a	chr8:91200101-91200110 chr8:91200100-91200109
42	BCLAF1	chr8:91233390-91234078	K562	blood:	n/a	n/a
43	BHLHE40	chr8:91178731-91178776	K562	blood:	n/a	n/a
44	BHLHE40	chr8:91233486-91234126	K562	blood:	n/a	n/a
45	BHLHE40	chr8:91209621-91209921	K562	blood:	n/a	n/a
46	BHLHE40	chr8:91094881-91095352	K562	blood:	n/a	n/a
47	BHLHE40	chr8:91179764-91180598	K562	blood:	n/a	n/a
48	BHLHE40	chr8:91184139-91184423	K562	blood:	n/a	n/a
49	BHLHE40	chr8:91206506-91206701	K562	blood:	n/a	n/a
50	BHLHE40	chr8:91223843-91224123	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:91094422-91094472	AG09309	skin:	n/a
2	chr8:91094847-91094897	AG04450	lung:	fetal
3	chr8:91227102-91227152	HCPEpiC	choroid plexus:	n/a
4	chr8:91099036-91099086	NT2-D1	testis:	n/a
5	chr8:91108620-91108670	Caco-2	colon:	n/a
6	chr8:91095906-91095956	K562	blood:	n/a
7	chr8:91173192-91173242	HCT-116	colon:	n/a
8	chr8:91173192-91173242	HRPEpiC	eye:	n/a
9	chr8:91095058-91095108	SKMC	muscle:	n/a
10	chr8:91094472-91094522	T-47D	breast:	n/a
11	chr8:91095114-91095164	NH-A	brain:	n/a
12	chr8:91095114-91095164	GM12878	blood:	n/a
13	chr8:91108188-91108238	SK-N-SH_RA	brain:	n/a
14	chr8:91094547-91094597	Hela-S3	cervix:	n/a
15	chr8:91108620-91108670	HRPEpiC	eye:	n/a
16	chr8:91108188-91108238	HL-60	blood:	n/a
17	chr8:91108188-91108238	GM12892	blood:	n/a
18	chr8:91094847-91094897	SK-N-SH	brain:	n/a
19	chr8:91094422-91094472	NHBE	bronchial:	n/a
20	chr8:91122625-91122675	A549	lung:	n/a
21	chr8:91094422-91094472	HAEpiC	amniotic membrane:	n/a
22	chr8:91094547-91094597	BJ	skin:	n/a
23	chr8:91173192-91173242	HAEpiC	amniotic membrane:	n/a
24	chr8:91094547-91094597	Caco-2	colon:	n/a
25	chr8:91122625-91122675	BE2_C	brain:	n/a
26	chr8:91094811-91094861	Caco-2	colon:	n/a
27	chr8:91094847-91094897	ECC-1	luminal epithelium:	n/a
28	chr8:91122625-91122675	NB4	blood:	n/a
29	chr8:91227102-91227152	IMR90	lung:	fetal
30	chr8:91173192-91173242	CMK	blood:	n/a
31	chr8:91095058-91095108	Jurkat	blood:	n/a
32	chr8:91108620-91108670	HIPEpiC	eye:	n/a
33	chr8:91094472-91094522	HRE	kidney:	n/a
34	chr8:91094422-91094472	Jurkat	blood:	n/a
35	chr8:91173192-91173242	AG09309	skin:	n/a
36	chr8:91094847-91094897	HRCEpiC	kidney:	n/a
37	chr8:91094847-91094897	GM12891	blood:	n/a
38	chr8:91099036-91099086	PANC-1	pancreas:	n/a
39	chr8:91108620-91108670	NHBE	bronchial:	n/a
40	chr8:91094472-91094522	SK-N-MC	brain:	n/a
41	chr8:91095114-91095164	K562	blood:	n/a
42	chr8:91094472-91094522	HEEpiC	esophagus:	n/a
43	chr8:91122625-91122675	NHDF-neo	bronchial:	n/a
44	chr8:91108620-91108670	BE2_C	brain:	n/a
45	chr8:91094547-91094597	HNPCEpiC	eye:	n/a
46	chr8:91095058-91095108	RPTEC	kidney:	n/a
47	chr8:91095058-91095108	IMR90	lung:	fetal
48	chr8:91094811-91094861	HEK293	kidney:	embryo
49	chr8:91095058-91095108	SK-N-MC	brain:	n/a
50	chr8:91094472-91094522	NT2-D1	testis:	n/a

(count:177 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:91180613..91183439-chr8:91193363..91195732,2	K562	blood:
2	chr8:91193596..91196355-chr8:91200011..91201961,2	K562	blood:
3	chr8:91210166..91212699-chr8:91233871..91237591,3	K562	blood:
4	chr8:91186436..91188660-chr8:91289229..91291075,2	K562	blood:
5	chr8:91195100..91196918-chr8:91207528..91209221,2	K562	blood:
6	chr8:91177486..91179176-chr8:91180628..91182984,2	K562	blood:
7	chr8:91208757..91210892-chr8:91218226..91220582,2	K562	blood:
8	chr8:91196434..91198632-chr8:91204961..91206870,2	K562	blood:
9	chr8:90993747..90995729-chr8:91225669..91228185,2	K562	blood:
10	chr8:91089800..91091325-chr8:91092595..91094860,2	MCF-7	breast:
11	chr8:91012457..91015215-chr8:91233847..91236431,2	K562	blood:
12	chr8:91180611..91183081-chr8:91185061..91187294,2	K562	blood:
13	chr10:103124108..103124630-chr8:91155315..91155836,3	HCT-116	colon:
14	chr8:91207463..91209619-chr8:91232587..91235024,2	K562	blood:
15	chr11:62607627..62609222-chr8:91155315..91156836,3	K562	blood:
16	chr8:91208888..91210489-chr8:91226599..91229382,2	K562	blood:
17	chr8:91085654..91087463-chr8:91095150..91097801,2	K562	blood:
18	chr11:62608628..62609148-chr8:91155315..91155836,4	NB4	blood:
19	chr8:91196894..91200069-chr8:91240130..91243292,3	K562	blood:
20	chr8:91177198..91178801-chr8:91185940..91187719,2	MCF-7	breast:
21	chr3:73158464..73161607-chr8:91155315..91156835,5	K562	blood:
22	chr8:91143386..91146044-chr8:91149940..91153117,3	K562	blood:
23	chr8:91186935..91188480-chr8:91190108..91192578,2	MCF-7	breast:
24	chr8:91208757..91210892-chr8:91218226..91220582,2	K562	blood:
25	chr8:91204870..91208091-chr8:91210126..91212391,3	K562	blood:
26	chr8:91196038..91198632-chr8:91205123..91206870,2	K562	blood:
27	chr1:245027270..245028019-chr8:91135650..91136189,2	MCF-7	breast:
28	chr17:41465192..41465706-chr8:91155316..91155835,2	HCT-116	colon:
29	chr8:91197950..91200166-chr8:91210110..91212853,2	K562	blood:
30	chr8:91228314..91231823-chr8:91238061..91241526,6	K562	blood:
31	chr8:91139396..91140972-chr8:91161545..91163760,2	K562	blood:
32	chr17:41463347..41467581-chr8:91153836..91156836,7	K562	blood:
33	chr8:91177720..91183484-chr8:91189779..91192790,4	K562	blood:
34	chr8:91147559..91149333-chr8:91149413..91151498,3	K562	blood:
35	chr8:91143386..91146044-chr8:91149940..91153117,3	K562	blood:
36	chr8:91177407..91179281-chr8:91196128..91199121,2	MCF-7	breast:
37	chr8:91155035..91157497-chr8:91163156..91166027,2	K562	blood:
38	chr3:73159863..73160626-chr8:91155316..91155835,2	MCF-7	breast:
39	chr8:91066837..91069760-chr8:91090559..91092238,2	K562	blood:
40	chr8:91180063..91181586-chr8:91247725..91249729,2	K562	blood:
41	chr8:91110151..91112011-chr8:91117979..91120218,2	K562	blood:
42	chr8:91013544..91014232-chr8:91093329..91094000,2	MCF-7	breast:
43	chr3:73160015..73161608-chr8:91155335..91156836,2	K562	blood:
44	chr8:91111364..91113093-chr8:91113728..91115750,2	K562	blood:
45	chr8:91160123..91162835-chr8:91174934..91176685,2	K562	blood:
46	chr8:91121306..91123004-chr8:91234013..91235686,2	K562	blood:
47	chr8:91121306..91123004-chr8:91234013..91235686,2	K562	blood:
48	chr8:91124236..91126354-chr8:91127708..91130462,3	K562	blood:
49	chr17:41400577..41402205-chr8:91155335..91156836,2	K562	blood:
50	chr8:91152980..91155385-chr8:91174154..91176618,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DECR1-1	chr8:91233716-91233974	NONHSAT127644
2	lnc-DECR1-1	chr8:91233766-91233974	ENSG00000253394
3	lnc-DECR1-1	chr8:91233716-91233738	ENSG00000253394
4	lnc-DECR1-1	chr8:91233745-91233974	ENSG00000253394
5	lnc-DECR1-1	chr8:91233716-91233974	ENSG00000253394
6	lnc-DECR1-1	chr8:91233875-91233974	ENSG00000253394

No data

Variant related genes	Relation type
LINC00534	TF binding region
CALB1	TF binding region
LINC00534	CpG island
CALB1	CpG island
ENSG00000104312	chromatin interactions
ENSG00000233016	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000104320	chromatin interactions
ENSG00000104325	chromatin interactions
ENSG00000074211	chromatin interactions
ENSG00000153187	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000104327	chromatin interactions
ENSG00000253394	chromatin interactions

Extended variants
information (count: 4319 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:4319 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16902840	chr8:91090821-91090822	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557897075	chr8:91090823-91090824	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566569529	chr8:91090832-91090833	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565048961	chr8:91090846-91090847	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs186714967	chr8:91090860-91090861	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs562777404	chr8:91090862-91090863	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs117918975	chr8:91090886-91090887	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs141636789	chr8:91090945-91090946	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541044106	chr8:91090992-91090993	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs115983428	chr8:91091020-91091021	Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs557471067	chr8:91091132-91091133	Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs575844076	chr8:91091139-91091140	Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559730912	chr8:91091158-91091159	Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545997016	chr8:91091233-91091234	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574706046	chr8:91091268-91091269	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374469273	chr8:91091340-91091341	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs10098170	chr8:91091402-91091403	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs548550553	chr8:91091419-91091420	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs528684183	chr8:91091449-91091450	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs192621671	chr8:91091570-91091571	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs183019716	chr8:91091776-91091777	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs530732241	chr8:91091782-91091783	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs528856430	chr8:91091844-91091845	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs550192859	chr8:91091867-91091868	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs562158240	chr8:91091875-91091876	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs532832632	chr8:91091901-91091902	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs551188103	chr8:91091943-91091944	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs563608999	chr8:91091993-91091994	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566620652	chr8:91092016-91092017	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs533787023	chr8:91092020-91092021	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs10755930	chr8:91092028-91092029	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs567593543	chr8:91092030-91092031	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs75272344	chr8:91092033-91092034	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs557359318	chr8:91092080-91092081	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs147073977	chr8:91092097-91092098	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs575730620	chr8:91092205-91092206	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs138258493	chr8:91092207-91092208	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs77798206	chr8:91092271-91092272	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs374269718	chr8:91092302-91092303	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs188100505	chr8:91092332-91092333	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs528241618	chr8:91092359-91092360	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs570473747	chr8:91092402-91092403	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs540519074	chr8:91092421-91092422	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs562024797	chr8:91092452-91092453	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs573959322	chr8:91092471-91092472	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs192680886	chr8:91092511-91092512	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs75069313	chr8:91092526-91092527	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs532799501	chr8:91092555-91092556	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs551446191	chr8:91092557-91092558	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs560035210	chr8:91092587-91092588	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
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
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91057800-91093600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:91068000-91093200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr8:91073400-91093600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr8:91075000-91091000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:91086000-91091400	Weak transcription	Brain Anterior Caudate	brain
6	chr8:91090800-91091600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:91091000-91091200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:91091200-91095400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:91091400-91094800	Active TSS	Brain Anterior Caudate	brain
10	chr8:91091600-91092000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:91092000-91092400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:91092400-91093000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:91093000-91093200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:91093200-91094000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
15	chr8:91093200-91094800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
16	chr8:91093200-91095400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:91093400-91093600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
18	chr8:91093400-91094000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:91093400-91095000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
20	chr8:91093600-91093800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr8:91093600-91093800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:91093600-91094000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
23	chr8:91093600-91094400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr8:91093600-91094800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
25	chr8:91093600-91095000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
26	chr8:91093600-91095200	Active TSS	H1 Cell Line	embryonic stem cell
27	chr8:91093600-91095200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr8:91093600-91095400	Active TSS	H9 Cell Line	embryonic stem cell
29	chr8:91093800-91094000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr8:91093800-91094200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
31	chr8:91093800-91094600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
32	chr8:91093800-91094600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
33	chr8:91094000-91094200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
34	chr8:91094000-91094200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr8:91094000-91094200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
36	chr8:91094000-91094200	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:91094000-91094200	Enhancers	Brain Hippocampus Middle	brain
38	chr8:91094000-91094200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr8:91094000-91094600	Bivalent Enhancer	Fetal Heart	heart
40	chr8:91094000-91094800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr8:91094000-91094800	Bivalent Enhancer	Brain Angular Gyrus	brain
42	chr8:91094000-91095000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
43	chr8:91094000-91095200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr8:91094000-91095200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr8:91094000-91095400	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr8:91094000-91095400	Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr8:91094200-91094400	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr8:91094200-91094400	Enhancers	Brain Substantia Nigra	brain
49	chr8:91094200-91094600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
50	chr8:91094200-91094800	Flanking Active TSS	Brain Hippocampus Middle	brain

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