Variant report

Variant	nsv1018791
Chromosome Location	chr8:69729491-69814849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:757)
CpG islands
(count:122)
Chromatin interactive
region (count:88)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:69766609-69766662	K562	blood:	n/a	n/a
2	BACH1	chr8:69754732-69754789	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr8:69766374-69766681	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr8:69807225-69807475	K562	blood:	n/a	n/a
5	CCNT2	chr8:69779720-69780000	K562	blood:	n/a	n/a
6	CEBPB	chr8:69775897-69776142	H1-hESC	embryonic stem cell:	n/a	chr8:69775990-69776001 chr8:69775988-69775999 chr8:69775988-69776001 chr8:69776013-69776030
7	CEBPB	chr8:69765552-69765896	IMR90	lung:	n/a	n/a
8	CEBPB	chr8:69784797-69785312	MCF-7	breast:	n/a	n/a
9	CEBPB	chr8:69810138-69810233	A549	lung:	n/a	n/a
10	CEBPB	chr8:69769702-69769994	ECC-1	luminal epithelium:	n/a	chr8:69769827-69769838
11	CEBPB	chr8:69766289-69767225	MCF-7	breast:	n/a	n/a
12	CEBPB	chr8:69787374-69787857	MCF-7	breast:	n/a	n/a
13	CEBPB	chr8:69765174-69766198	MCF-7	breast:	n/a	n/a
14	CEBPB	chr8:69769654-69770010	HepG2	liver:	n/a	chr8:69769827-69769838
15	CEBPB	chr8:69769649-69770020	K562	blood:	n/a	chr8:69769827-69769838
16	CEBPB	chr8:69775799-69776266	MCF-7	breast:	n/a	chr8:69775990-69776001 chr8:69775988-69775999 chr8:69775988-69776001 chr8:69776013-69776030
17	CEBPB	chr8:69775835-69776145	HepG2	liver:	n/a	chr8:69775990-69776001 chr8:69775988-69775999 chr8:69775988-69776001 chr8:69776013-69776030
18	CEBPB	chr8:69787449-69787842	MCF-7	breast:	n/a	n/a
19	CEBPB	chr8:69775817-69776229	MCF-7	breast:	n/a	chr8:69775990-69776001 chr8:69775988-69775999 chr8:69775988-69776001 chr8:69776013-69776030
20	CEBPB	chr8:69784865-69785286	MCF-7	breast:	n/a	n/a
21	CEBPB	chr8:69775850-69776105	A549	lung:	n/a	chr8:69775990-69776001 chr8:69775988-69775999 chr8:69775988-69776001 chr8:69776013-69776030
22	CEBPB	chr8:69765246-69766300	MCF-7	breast:	n/a	n/a
23	CEBPB	chr8:69766339-69767360	MCF-7	breast:	n/a	n/a
24	CEBPB	chr8:69765169-69766410	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:69769636-69770016	IMR90	lung:	n/a	chr8:69769827-69769838
26	CEBPB	chr8:69774486-69774902	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr8:69769650-69770006	H1-hESC	embryonic stem cell:	n/a	chr8:69769827-69769838
28	CEBPB	chr8:69756830-69756937	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr8:69769651-69769980	A549	lung:	n/a	chr8:69769827-69769838
30	CEBPB	chr8:69775797-69776231	Hela-S3	cervix:	n/a	chr8:69775990-69776001 chr8:69775988-69775999 chr8:69775988-69776001 chr8:69776013-69776030
31	CEBPB	chr8:69787408-69787796	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr8:69809596-69809806	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:69754683-69754791	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr8:69782218-69782373	A549	lung:	n/a	chr8:69782270-69782281
35	CEBPB	chr8:69782153-69782406	HepG2	liver:	n/a	chr8:69782270-69782281
36	CEBPB	chr8:69769593-69770088	MCF-7	breast:	n/a	chr8:69769827-69769838 chr8:69770067-69770080 chr8:69770067-69770079
37	CEBPB	chr8:69784865-69785223	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr8:69769657-69769982	Hela-S3	cervix:	n/a	chr8:69769827-69769838
39	CHD2	chr8:69762875-69763007	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr8:69766420-69766570	GM12865	blood:	n/a	chr8:69766507-69766528 chr8:69766505-69766523
41	CTCF	chr8:69766480-69766630	GM12871	blood:	n/a	chr8:69766507-69766528 chr8:69766505-69766523
42	CTCF	chr8:69766340-69766490	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr8:69755846-69755930	HepG2	liver:	n/a	chr8:69755893-69755909
44	CTCF	chr8:69755789-69756025	GM12878	blood:	n/a	chr8:69755893-69755909
45	CTCF	chr8:69766460-69766610	GM12865	blood:	n/a	chr8:69766507-69766528 chr8:69766505-69766523
46	CTCF	chr8:69755820-69755970	HepG2	liver:	n/a	chr8:69755893-69755909
47	CTCF	chr8:69755820-69755970	SK-N-SH_RA	brain:	n/a	chr8:69755893-69755909
48	CTCF	chr8:69766420-69766570	HVMF	connective:	n/a	chr8:69766507-69766528 chr8:69766505-69766523
49	CTCF	chr8:69766440-69766590	HRPEpiC	eye:	n/a	chr8:69766507-69766528 chr8:69766505-69766523
50	CTCF	chr8:69766337-69766670	HUVEC	blood vessel:	n/a	chr8:69766507-69766528 chr8:69766505-69766523

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:69755069-69755119	HEK293	kidney:	embryo
2	chr8:69781040-69781090	Jurkat	blood:	n/a
3	chr8:69755069-69755119	HIPEpiC	eye:	n/a
4	chr8:69781040-69781090	ProgFib	skin:	n/a
5	chr8:69781040-69781090	GM19239	blood:	n/a
6	chr8:69781040-69781090	U87	brain:	n/a
7	chr8:69781040-69781090	AG09309	skin:	n/a
8	chr8:69755069-69755119	GM12891	blood:	n/a
9	chr8:69781040-69781090	BE2_C	brain:	n/a
10	chr8:69781040-69781090	HCT-116	colon:	n/a
11	chr8:69781040-69781090	GM12878	blood:	n/a
12	chr8:69781040-69781090	ovcar-3	ovarian:	n/a
13	chr8:69755069-69755119	T-47D	breast:	n/a
14	chr8:69755069-69755119	Jurkat	blood:	n/a
15	chr8:69781040-69781090	K562	blood:	n/a
16	chr8:69755069-69755119	HMEC	breast:	n/a
17	chr8:69755069-69755119	K562	blood:	n/a
18	chr8:69781040-69781090	IMR90	lung:	fetal
19	chr8:69755069-69755119	PrEC	prostate:	n/a
20	chr8:69755069-69755119	H1-hESC	embryonic stem cell:	embryo
21	chr8:69755069-69755119	GM12878	blood:	n/a
22	chr8:69755069-69755119	HEEpiC	esophagus:	n/a
23	chr8:69781040-69781090	A549	lung:	n/a
24	chr8:69755069-69755119	A549	lung:	n/a
25	chr8:69755069-69755119	NB4	blood:	n/a
26	chr8:69781040-69781090	LNCaP	prostate:	n/a
27	chr8:69755069-69755119	GM19239	blood:	n/a
28	chr8:69781040-69781090	CMK	blood:	n/a
29	chr8:69755069-69755119	HPAEpiC	pulmonary alveolar:	n/a
30	chr8:69781040-69781090	HNPCEpiC	eye:	n/a
31	chr8:69755069-69755119	HL-60	blood:	n/a
32	chr8:69755069-69755119	SAEC	small airway:	n/a
33	chr8:69781040-69781090	RPTEC	kidney:	n/a
34	chr8:69781040-69781090	HIPEpiC	eye:	n/a
35	chr8:69781040-69781090	HRPEpiC	eye:	n/a
36	chr8:69755069-69755119	ECC-1	luminal epithelium:	n/a
37	chr8:69755069-69755119	PFSK-1	brain:	n/a
38	chr8:69781040-69781090	HRCEpiC	kidney:	n/a
39	chr8:69755069-69755119	HCM	heart:	n/a
40	chr8:69755069-69755119	Hela-S3	cervix:	n/a
41	chr8:69755069-69755119	RPTEC	kidney:	n/a
42	chr8:69755069-69755119	HCF	heart:	n/a
43	chr8:69781040-69781090	SAEC	small airway:	n/a
44	chr8:69755069-69755119	SKMC	muscle:	n/a
45	chr8:69781040-69781090	AG04449	skin:	fetal
46	chr8:69755069-69755119	HNPCEpiC	eye:	n/a
47	chr8:69781040-69781090	SKMC	muscle:	n/a
48	chr8:69755069-69755119	NH-A	brain:	n/a
49	chr8:69755069-69755119	BE2_C	brain:	n/a
50	chr8:69755069-69755119	HRPEpiC	eye:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:69740378..69741193-chr8:69766698..69767308,2	MCF-7	breast:
2	chr8:69766183..69766998-chr8:70468234..70468991,2	MCF-7	breast:
3	chr8:69766577..69767096-chr8:69938024..69938567,2	MCF-7	breast:
4	chr8:69749429..69752254-chr8:69754411..69757216,3	MCF-7	breast:
5	chr8:69725101..69728063-chr8:69734380..69737954,3	MCF-7	breast:
6	chr8:69747162..69748788-chr8:69755225..69758210,2	MCF-7	breast:
7	chr8:69758461..69760181-chr8:69760433..69761977,2	MCF-7	breast:
8	chr8:69783987..69786216-chr8:69786621..69791485,4	MCF-7	breast:
9	chr8:69762068..69763713-chr8:70060193..70062538,2	MCF-7	breast:
10	chr8:69740233..69741132-chr8:69765307..69766148,2	MCF-7	breast:
11	chr8:69747162..69748788-chr8:69755225..69758210,2	MCF-7	breast:
12	chr8:69773675..69775260-chr8:70017134..70019625,2	MCF-7	breast:
13	chr8:69338439..69340713-chr8:69760510..69763451,2	MCF-7	breast:
14	chr8:69762264..69763807-chr8:69938743..69941277,2	MCF-7	breast:
15	chr8:69813641..69815501-chr8:69817466..69820141,2	MCF-7	breast:
16	chr8:69610109..69611975-chr8:69765057..69767019,2	MCF-7	breast:
17	chr8:69765041..69767952-chr8:69838126..69840398,3	MCF-7	breast:
18	chr8:69774615..69776136-chr8:69778095..69779612,2	MCF-7	breast:
19	chr8:69766996..69770289-chr8:69772994..69775447,3	MCF-7	breast:
20	chr8:69766399..69767115-chr8:69991782..69992767,2	MCF-7	breast:
21	chr8:69766511..69767277-chr8:70023631..70024260,3	MCF-7	breast:
22	chr8:69766369..69767301-chr8:70023597..70024512,9	MCF-7	breast:
23	chr8:69781287..69782910-chr8:69784282..69786864,2	MCF-7	breast:
24	chr8:69754552..69756282-chr8:69983861..69986611,2	MCF-7	breast:
25	chr8:69766557..69767484-chr8:69984843..69985678,2	MCF-7	breast:
26	chr8:69738712..69740875-chr8:69761908..69763896,2	MCF-7	breast:
27	chr8:69766441..69769103-chr8:69782417..69786375,4	MCF-7	breast:
28	chr8:69611388..69613442-chr8:69760561..69763282,2	MCF-7	breast:
29	chr8:69753329..69755491-chr8:69758339..69760830,2	MCF-7	breast:
30	chr8:69766441..69769103-chr8:69782417..69786375,4	MCF-7	breast:
31	chr8:69762198..69770207-chr8:70021083..70026192,14	MCF-7	breast:
32	chr8:69762270..69764090-chr8:70396514..70399312,2	MCF-7	breast:
33	chr8:69729862..69732117-chr8:69739416..69741955,2	MCF-7	breast:
34	chr8:69783987..69786216-chr8:69786621..69791485,4	MCF-7	breast:
35	chr8:69534291..69534942-chr8:69765230..69765734,2	MCF-7	breast:
36	chr8:69765267..69766228-chr8:70023907..70024508,4	MCF-7	breast:
37	chr8:69765117..69767304-chr8:69979220..69980795,2	MCF-7	breast:
38	chr8:69778375..69780629-chr8:69861166..69863483,2	MCF-7	breast:
39	chr8:69781287..69782910-chr8:69784282..69786864,2	MCF-7	breast:
40	chr8:69765267..69766228-chr8:70023563..70024508,7	MCF-7	breast:
41	chr8:69737474..69739792-chr8:69742930..69745719,2	MCF-7	breast:
42	chr8:69766578..69767279-chr8:69937764..69938297,2	MCF-7	breast:
43	chr8:69765805..69766693-chr8:69985208..69986080,2	MCF-7	breast:
44	chr8:69729862..69732117-chr8:69739416..69741955,2	MCF-7	breast:
45	chr8:69740233..69741132-chr8:69765307..69766148,2	MCF-7	breast:
46	chr8:69765354..69768313-chr8:70403823..70406098,3	MCF-7	breast:
47	chr8:69766547..69767337-chr8:69937588..69938663,4	MCF-7	breast:
48	chr8:69791453..69793746-chr8:69832544..69834116,2	MCF-7	breast:
49	chr8:69765987..69767833-chr8:69983718..69985913,2	MCF-7	breast:
50	chr8:69724187..69726479-chr8:69730901..69733190,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-664D7.4.1-2	chr8:69764936-69764998	ENSG00000254337
2	lnc-RP11-664D7.4.1-2	chr8:69762186-69762280	ENSG00000254337
3	lnc-RP11-664D7.4.1-2	chr8:69760977-69761333	ENSG00000254337

No data

Variant related genes	Relation type
ENSG00000254337	TF binding region
ENSG00000254337	CpG island
ENSG00000238808	chromatin interactions
ENSG00000254337	chromatin interactions
ENSG00000137573	chromatin interactions

Extended variants
information (count: 3073 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3073 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192466956	chr8:69729494-69729495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372547507	chr8:69729505-69729506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2958326	chr8:69729569-69729570	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs377441569	chr8:69729635-69729636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371159377	chr8:69729659-69729660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554890110	chr8:69729697-69729698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73285479	chr8:69729719-69729720	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs374590712	chr8:69729720-69729721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537188731	chr8:69729729-69729730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145192839	chr8:69729738-69729739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576828958	chr8:69729754-69729755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544874211	chr8:69729759-69729760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs17482603	chr8:69729812-69729813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs10109701	chr8:69729966-69729967	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs541218347	chr8:69729973-69729974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560966561	chr8:69729998-69729999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184031744	chr8:69729999-69730000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549616502	chr8:69730021-69730022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569672055	chr8:69730023-69730024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187259407	chr8:69730043-69730044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532163423	chr8:69730055-69730056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2958327	chr8:69730064-69730065	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs566352344	chr8:69730084-69730085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528829047	chr8:69730099-69730100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114155156	chr8:69730121-69730122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148718073	chr8:69730176-69730177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200003072	chr8:69730223-69730224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75596981	chr8:69730225-69730226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373457502	chr8:69730226-69730227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74695727	chr8:69730227-69730228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs16935104	chr8:69730286-69730287	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs142308664	chr8:69730290-69730291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191977861	chr8:69730298-69730299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540852446	chr8:69730327-69730328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146823160	chr8:69730332-69730333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552996524	chr8:69730380-69730381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184577080	chr8:69730420-69730421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370122163	chr8:69730423-69730424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371656510	chr8:69730429-69730430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs16935106	chr8:69730432-69730433	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs574571750	chr8:69730464-69730465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs267601979	chr8:69730480-69730481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs16935109	chr8:69730488-69730489	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs375815398	chr8:69730491-69730492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563354083	chr8:69730497-69730498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376421977	chr8:69730570-69730571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545809990	chr8:69730587-69730588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574638409	chr8:69730629-69730630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559429875	chr8:69730645-69730646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs58046094	chr8:69730661-69730662	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:101)

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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69722600-69734200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:69732000-69732600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:69732400-69732600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:69732400-69732600	Enhancers	Fetal Brain Male	brain
5	chr8:69732600-69734200	Weak transcription	Fetal Brain Male	brain
6	chr8:69734200-69736000	Enhancers	Fetal Brain Male	brain
7	chr8:69734800-69736200	Enhancers	Fetal Lung	lung
8	chr8:69736000-69742200	Weak transcription	Fetal Brain Male	brain
9	chr8:69736200-69741400	Weak transcription	Fetal Lung	lung
10	chr8:69741400-69743200	Enhancers	Fetal Lung	lung
11	chr8:69741600-69742400	Enhancers	Colon Smooth Muscle	Colon
12	chr8:69741600-69742600	Enhancers	Hela-S3	cervix
13	chr8:69741600-69743200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr8:69741800-69742200	Weak transcription	NHLF	lung
15	chr8:69742000-69742200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr8:69742000-69742200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:69742000-69742200	Enhancers	Liver	Liver
18	chr8:69742000-69742600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr8:69742000-69742600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr8:69742000-69742600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr8:69742000-69742600	Active TSS	NHEK	skin
22	chr8:69742000-69742600	Active TSS	Osteobl	bone
23	chr8:69742200-69742400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:69742200-69742400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:69742200-69742600	Active TSS	Fetal Brain Male	brain
26	chr8:69742200-69742600	Active TSS	NHLF	lung
27	chr8:69742200-69742800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:69742200-69743200	Flanking Active TSS	Liver	Liver
29	chr8:69742400-69742600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr8:69742400-69742600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr8:69742400-69742800	Flanking Active TSS	Colon Smooth Muscle	Colon
32	chr8:69742600-69742800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr8:69742600-69744200	Weak transcription	Hela-S3	cervix
34	chr8:69742800-69743000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr8:69742800-69743000	Enhancers	Colon Smooth Muscle	Colon
36	chr8:69743200-69743600	Enhancers	Liver	Liver
37	chr8:69751000-69751400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:69751200-69751400	Weak transcription	Aorta	Aorta
39	chr8:69751200-69758600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr8:69751400-69751600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr8:69751400-69751600	Enhancers	Aorta	Aorta
42	chr8:69751400-69752600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr8:69751600-69752800	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr8:69751600-69762800	Weak transcription	Aorta	Aorta
45	chr8:69752400-69757800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr8:69752600-69754400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr8:69752600-69754800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr8:69752600-69755200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr8:69752600-69756000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr8:69752800-69753400	Enhancers	H9 Cell Line	embryonic stem cell

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