Variant report

Variant	nsv1031578
Chromosome Location	chr8:90670102-90757821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1221)
CpG islands
(count:61)
Chromatin interactive
region (count:97)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1221 , 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	chr8:90742157-90742510	K562	blood:	n/a	n/a
2	ARID3A	chr8:90738074-90738343	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:90741133-90741702	K562	blood:	n/a	n/a
4	ARID3A	chr8:90730496-90730904	K562	blood:	n/a	n/a
5	ARID3A	chr8:90738052-90738327	K562	blood:	n/a	n/a
6	ARID3A	chr8:90732814-90733099	HepG2	liver:	n/a	n/a
7	ATF1	chr8:90738051-90738334	K562	blood:	n/a	n/a
8	ATF1	chr8:90740926-90741719	K562	blood:	n/a	n/a
9	ATF2	chr8:90737920-90738636	GM12878	blood:	n/a	n/a
10	ATF2	chr8:90741902-90742786	GM12878	blood:	n/a	n/a
11	ATF2	chr8:90741233-90741894	GM12878	blood:	n/a	n/a
12	ATF2	chr8:90738026-90738427	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr8:90741953-90742740	GM12878	blood:	n/a	n/a
14	ATF2	chr8:90732722-90733233	GM12878	blood:	n/a	n/a
15	ATF2	chr8:90732595-90733323	GM12878	blood:	n/a	n/a
16	ATF2	chr8:90737929-90738551	GM12878	blood:	n/a	n/a
17	ATF2	chr8:90741207-90741815	GM12878	blood:	n/a	n/a
18	BACH1	chr8:90738096-90738310	K562	blood:	n/a	n/a
19	BACH1	chr8:90738733-90738759	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr8:90738003-90738500	GM12878	blood:	n/a	chr8:90738291-90738302 chr8:90738292-90738302
21	BATF	chr8:90741449-90741737	GM12878	blood:	n/a	n/a
22	BATF	chr8:90742327-90742620	GM12878	blood:	n/a	n/a
23	BATF	chr8:90732830-90733137	GM12878	blood:	n/a	n/a
24	BATF	chr8:90738011-90738449	GM12878	blood:	n/a	chr8:90738291-90738302 chr8:90738292-90738302
25	BATF	chr8:90750493-90750763	GM12878	blood:	n/a	n/a
26	BATF	chr8:90742356-90742616	GM12878	blood:	n/a	n/a
27	BATF	chr8:90741444-90741729	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:90741404-90741705	GM12878	blood:	n/a	n/a
29	BCL3	chr8:90737989-90738504	GM12878	blood:	n/a	chr8:90738122-90738131
30	BCL3	chr8:90732736-90733192	GM12878	blood:	n/a	n/a
31	BCLAF1	chr8:90742189-90742602	GM12878	blood:	n/a	chr8:90742261-90742270
32	BCLAF1	chr8:90741285-90741840	GM12878	blood:	n/a	n/a
33	BCLAF1	chr8:90737861-90738551	GM12878	blood:	n/a	chr8:90738122-90738131 chr8:90737903-90737912
34	BCLAF1	chr8:90737957-90738469	GM12878	blood:	n/a	chr8:90738122-90738131
35	BHLHE40	chr8:90738028-90738733	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:90741068-90741648	K562	blood:	n/a	n/a
37	BHLHE40	chr8:90740597-90740708	GM12878	blood:	n/a	n/a
38	BHLHE40	chr8:90738026-90738384	K562	blood:	n/a	n/a
39	BHLHE40	chr8:90741301-90741779	GM12878	blood:	n/a	n/a
40	BHLHE40	chr8:90733984-90734101	K562	blood:	n/a	n/a
41	BHLHE40	chr8:90701446-90701737	GM12878	blood:	n/a	n/a
42	BRCA1	chr8:90717312-90717508	GM12878	blood:	n/a	n/a
43	BRCA1	chr8:90741488-90741644	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr8:90748284-90748626	K562	blood:	n/a	n/a
45	CBX3	chr8:90740890-90741741	K562	blood:	n/a	n/a
46	CBX3	chr8:90737999-90738365	K562	blood:	n/a	n/a
47	CCNT2	chr8:90741406-90741610	K562	blood:	n/a	n/a
48	CEBPB	chr8:90710100-90710300	A549	lung:	n/a	chr8:90710214-90710225
49	CEBPB	chr8:90732828-90733233	HepG2	liver:	n/a	n/a
50	CEBPB	chr8:90701408-90701703	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90730638-90730688	GM12878	blood:	n/a
2	chr8:90730638-90730688	K562	blood:	n/a
3	chr8:90730638-90730688	LNCaP	prostate:	n/a
4	chr8:90730638-90730688	PrEC	prostate:	n/a
5	chr8:90730638-90730688	T-47D	breast:	n/a
6	chr8:90730638-90730688	CMK	blood:	n/a
7	chr8:90730638-90730688	GM06990	blood:	n/a
8	chr8:90730638-90730688	SK-N-SH	brain:	n/a
9	chr8:90730638-90730688	HRPEpiC	eye:	n/a
10	chr8:90730638-90730688	Hela-S3	cervix:	n/a
11	chr8:90730638-90730688	HEEpiC	esophagus:	n/a
12	chr8:90730638-90730688	Caco-2	colon:	n/a
13	chr8:90730638-90730688	GM12892	blood:	n/a
14	chr8:90730638-90730688	AG10803	skin:	n/a
15	chr8:90730638-90730688	HL-60	blood:	n/a
16	chr8:90730638-90730688	NH-A	brain:	n/a
17	chr8:90730638-90730688	Jurkat	blood:	n/a
18	chr8:90730638-90730688	HUVEC	blood vessel:	n/a
19	chr8:90730638-90730688	AG09309	skin:	n/a
20	chr8:90730638-90730688	HEK293	kidney:	embryo
21	chr8:90730638-90730688	HCF	heart:	n/a
22	chr8:90730638-90730688	HIPEpiC	eye:	n/a
23	chr8:90730638-90730688	U87	brain:	n/a
24	chr8:90730638-90730688	AG09319	gingival:	n/a
25	chr8:90730638-90730688	HRCEpiC	kidney:	n/a
26	chr8:90730638-90730688	ovcar-3	ovarian:	n/a
27	chr8:90730638-90730688	BE2_C	brain:	n/a
28	chr8:90730638-90730688	Hepatocyte	liver:	n/a
29	chr8:90730638-90730688	HepG2	liver:	n/a
30	chr8:90730638-90730688	SK-N-MC	brain:	n/a
31	chr8:90730638-90730688	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:90730638-90730688	HRE	kidney:	n/a
33	chr8:90730638-90730688	PFSK-1	brain:	n/a
34	chr8:90730638-90730688	GM12891	blood:	n/a
35	chr8:90730638-90730688	AG04450	lung:	fetal
36	chr8:90730638-90730688	HAEpiC	amniotic membrane:	n/a
37	chr8:90730638-90730688	A549	lung:	n/a
38	chr8:90730638-90730688	IMR90	lung:	fetal
39	chr8:90730638-90730688	NHBE	bronchial:	n/a
40	chr8:90730638-90730688	SK-N-SH_RA	brain:	n/a
41	chr8:90730638-90730688	BJ	skin:	n/a
42	chr8:90730638-90730688	NB4	blood:	n/a
43	chr8:90730638-90730688	ECC-1	luminal epithelium:	n/a
44	chr8:90730638-90730688	H1-hESC	embryonic stem cell:	embryo
45	chr8:90730638-90730688	MCF10A-Er-Src	breast:	n/a
46	chr8:90730638-90730688	HNPCEpiC	eye:	n/a
47	chr8:90730638-90730688	SKMC	muscle:	n/a
48	chr8:90730638-90730688	RPTEC	kidney:	n/a
49	chr8:90730638-90730688	ProgFib	skin:	n/a
50	chr8:90730638-90730688	MCF-7	breast:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:90756480..90757980-chr8:90764220..90765823,2	K562	blood:
2	chr8:90753685..90756450-chr8:90766720..90768459,2	MCF-7	breast:
3	chr8:90730098..90733347-chr8:90733512..90737608,4	MCF-7	breast:
4	chr8:90731255..90734229-chr8:90770926..90773381,2	MCF-7	breast:
5	chr8:90730227..90732540-chr8:90735572..90739536,4	MCF-7	breast:
6	chr8:90730221..90731273-chr8:91007539..91008842,5	MCF-7	breast:
7	chr8:90741234..90743922-chr8:90995229..90998004,3	MCF-7	breast:
8	chr8:90742416..90744281-chr8:90745142..90746926,3	MCF-7	breast:
9	chr8:90757406..90760998-chr8:90767519..90771455,4	MCF-7	breast:
10	chr8:90740620..90742197-chr8:90743722..90745998,2	K562	blood:
11	chr8:90729414..90732733-chr8:91011369..91014401,3	MCF-7	breast:
12	chr8:90732834..90736227-chr8:90736670..90741646,5	MCF-7	breast:
13	chr8:90738830..90741040-chr8:90913929..90916655,2	K562	blood:
14	chr8:90738336..90739847-chr8:90952483..90954708,2	MCF-7	breast:
15	chr8:90736815..90743993-chr8:90765696..90773918,18	MCF-7	breast:
16	chr8:90265140..90266864-chr8:90701198..90702017,6	MCF-7	breast:
17	chr8:90740691..90742554-chr8:91012981..91015197,3	MCF-7	breast:
18	chr17:36869922..36870448-chr8:90717364..90718185,2	MCF-7	breast:
19	chr8:90732925..90737686-chr8:90738407..90742912,6	K562	blood:
20	chr8:90409684..90410477-chr8:90701050..90701985,2	MCF-7	breast:
21	chr8:90727118..90729538-chr8:90730165..90731877,3	MCF-7	breast:
22	chr8:90750906..90752567-chr8:90769734..90771633,2	MCF-7	breast:
23	chr8:90735826..90740064-chr8:90995306..90998250,3	MCF-7	breast:
24	chr8:90727781..90733734-chr8:90995200..90998684,11	MCF-7	breast:
25	chr8:90737750..90738653-chr8:90995891..90997375,11	MCF-7	breast:
26	chr8:90730473..90731451-chr8:90996501..90997250,3	K562	blood:
27	chr8:90742416..90744281-chr8:90745142..90746926,3	MCF-7	breast:
28	chr8:90727232..90729258-chr8:90996337..90998108,2	K562	blood:
29	chr8:90707734..90710584-chr8:90712902..90714410,2	K562	blood:
30	chr8:89930914..89931750-chr8:90701140..90701846,2	MCF-7	breast:
31	chr8:90727118..90729538-chr8:90730165..90731877,3	MCF-7	breast:
32	chr8:90738912..90741485-chr8:91017416..91019883,2	K562	blood:
33	chr8:90739799..90743850-chr8:90767861..90774313,11	K562	blood:
34	chr8:90701508..90704091-chr8:90704725..90706436,2	MCF-7	breast:
35	chr8:90701576..90703155-chr8:90704849..90706858,2	K562	blood:
36	chr8:90735002..90740593-chr8:90994599..90998168,11	MCF-7	breast:
37	chr8:90737986..90738708-chr8:90849422..90850036,2	MCF-7	breast:
38	chr8:87715292..87715843-chr8:90701514..90702072,2	K562	blood:
39	chr8:90674028..90676742-chr8:90677317..90680172,3	K562	blood:
40	chr8:90671410..90675466-chr8:90680458..90682318,3	K562	blood:
41	chr8:90735006..90737562-chr8:90957378..90959199,2	MCF-7	breast:
42	chr8:90752983..90756516-chr8:90768798..90771360,4	MCF-7	breast:
43	chr8:90265298..90266142-chr8:90701378..90702003,2	MCF-7	breast:
44	chr8:90677064..90679784-chr8:90680421..90682775,2	MCF-7	breast:
45	chr8:90739799..90744088-chr8:90767861..90774313,10	K562	blood:
46	chr8:90740620..90742197-chr8:90743722..90745998,2	K562	blood:
47	chr8:90271425..90272074-chr8:90701116..90702018,2	MCF-7	breast:
48	chr8:90714137..90717056-chr8:90737564..90740115,2	K562	blood:
49	chr8:90749748..90752499-chr8:90768284..90771226,3	MCF-7	breast:
50	chr8:90700247..90703773-chr8:90768935..90771399,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBN-1	chr8:90733132-90733602	ENSG00000251136
2	lnc-NBN-1	chr8:90734243-90734384	ENSG00000251136
3	lnc-NBN-1	chr8:90735244-90735764	NONHSAT127622
4	lnc-NBN-1	chr8:90736857-90737158	ENSG00000251136
5	lnc-NBN-1	chr8:90734243-90734578	NONHSAT127622
6	lnc-NBN-1	chr8:90737746-90737869	ENSG00000251136
7	lnc-NBN-1	chr8:90729627-90733428	ENSG00000251136
8	lnc-NBN-1	chr8:90732820-90733604	NONHSAT127622
9	lnc-NBN-1	chr8:90736857-90737194	NONHSAT127622
10	lnc-NBN-1	chr8:90736857-90737194	ENSG00000251136
11	lnc-NBN-1	chr8:90734243-90734384	ENSG00000251136
12	lnc-NBN-1	chr8:90737746-90737871	NONHSAT127622
13	lnc-NBN-1	chr8:90733172-90733602	ENSG00000251136
14	lnc-NBN-1	chr8:90729656-90729956	ENSG00000251136
15	lnc-NBN-1	chr8:90734243-90734578	ENSG00000251136

No data

Variant related genes	Relation type
ENSG00000251136	TF binding region
ENSG00000251136	CpG island
ENSG00000104325	chromatin interactions
ENSG00000207359	chromatin interactions
ENSG00000164823	chromatin interactions
ENSG00000104320	chromatin interactions
ENSG00000251136	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000104312	chromatin interactions
ENSG00000154217	chromatin interactions
KLK6	miRNA target sites
RGPD6	miRNA target sites
HMGA2	miRNA target sites
TMEM214	miRNA target sites
TPM3	miRNA target sites
DPH1	miRNA target sites
BCL2	miRNA target sites
CADM1	miRNA target sites

Extended variants
information (count: 3461 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:3461 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10956191	chr8:90670102-90670103	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545427862	chr8:90670124-90670125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564085785	chr8:90670160-90670161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147981408	chr8:90670166-90670167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547283911	chr8:90670174-90670175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562200159	chr8:90670178-90670179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529843910	chr8:90670183-90670184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529535695	chr8:90670249-90670250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551160681	chr8:90670267-90670268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140659441	chr8:90670297-90670298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534891040	chr8:90670299-90670300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553001181	chr8:90670319-90670320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539920778	chr8:90670326-90670327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551529575	chr8:90670329-90670330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574364833	chr8:90670363-90670364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182793172	chr8:90670419-90670420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187477744	chr8:90670468-90670469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72669912	chr8:90670472-90670473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190812523	chr8:90670500-90670501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183690148	chr8:90670534-90670535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142868459	chr8:90670536-90670537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535280803	chr8:90670558-90670559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556719326	chr8:90670622-90670623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs160423	chr8:90670623-90670624	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs545875688	chr8:90670625-90670626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs160424	chr8:90670680-90670681	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs115738513	chr8:90670690-90670691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539821914	chr8:90670770-90670771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145901855	chr8:90670778-90670779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs717580	chr8:90670785-90670786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564309610	chr8:90670786-90670787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551224558	chr8:90670791-90670792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138461728	chr8:90670792-90670793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376262691	chr8:90670795-90670796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs160425	chr8:90670803-90670804	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs565735498	chr8:90670815-90670816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374734279	chr8:90670837-90670838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551861202	chr8:90670844-90670845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566804823	chr8:90670845-90670846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534219443	chr8:90670846-90670847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527334392	chr8:90670849-90670850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549071316	chr8:90670850-90670851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568045075	chr8:90670851-90670852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188614120	chr8:90670870-90670871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs193267500	chr8:90670913-90670914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575108836	chr8:90670930-90670931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539213795	chr8:90670946-90670947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115074162	chr8:90670980-90670981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs160426	chr8:90671024-90671025	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs142983637	chr8:90671133-90671134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Bipolar disorder	19114987	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:900 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90665200-90675200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:90671000-90671200	Enhancers	Fetal Kidney	kidney
3	chr8:90671200-90671600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:90671200-90672000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:90671400-90675200	Weak transcription	Fetal Kidney	kidney
6	chr8:90671600-90672000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr8:90672000-90673400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:90673400-90674600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:90673600-90674400	Enhancers	NHDF-Ad	bronchial
10	chr8:90674000-90674200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr8:90674000-90675000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:90674000-90675200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr8:90674200-90675200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr8:90674400-90676000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:90675200-90675600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr8:90675200-90675800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:90675200-90675800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr8:90675200-90675800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:90675200-90676000	ZNF genes & repeats	Brain Hippocampus Middle	brain
20	chr8:90675200-90676000	ZNF genes & repeats	Pancreas	Pancrea
21	chr8:90675200-90676200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr8:90675800-90684800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:90676000-90690600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:90676000-90690600	Weak transcription	Pancreas	Pancrea
25	chr8:90676600-90677000	ZNF genes & repeats	Aorta	Aorta
26	chr8:90676600-90681400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:90677000-90684600	Weak transcription	Aorta	Aorta
28	chr8:90677600-90677800	Enhancers	Colon Smooth Muscle	Colon
29	chr8:90677800-90681200	Weak transcription	Colon Smooth Muscle	Colon
30	chr8:90678000-90681200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:90679200-90679400	Enhancers	Fetal Stomach	stomach
32	chr8:90679400-90681000	Weak transcription	Fetal Stomach	stomach
33	chr8:90679800-90680000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr8:90679800-90680000	Enhancers	Left Ventricle	heart
35	chr8:90679800-90682400	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr8:90680000-90681000	Weak transcription	Left Ventricle	heart
37	chr8:90681000-90681800	Enhancers	Left Ventricle	heart
38	chr8:90681000-90682200	Enhancers	Fetal Stomach	stomach
39	chr8:90681200-90682000	Enhancers	Colon Smooth Muscle	Colon
40	chr8:90681400-90681600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr8:90681400-90681800	Enhancers	Fetal Lung	lung
42	chr8:90681600-90682000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr8:90681600-90682000	Enhancers	Ovary	ovary
44	chr8:90681600-90682000	Enhancers	Right Atrium	heart
45	chr8:90682000-90682200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:90682000-90690600	Weak transcription	Ovary	ovary
47	chr8:90682200-90686200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr8:90682800-90687200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr8:90684600-90684800	ZNF genes & repeats	Aorta	Aorta
50	chr8:90684800-90685400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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