Variant report

Variant	nsv890359
Chromosome Location	chr8:11599570-11617240
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:11603906-11604207	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr8:11603768-11604225	GM12878	blood:	n/a	n/a
3	BHLHE40	chr8:11606456-11606707	K562	blood:	n/a	chr8:11606598-11606607 chr8:11606598-11606607 chr8:11606599-11606608
4	BHLHE40	chr8:11614179-11614527	K562	blood:	n/a	chr8:11614317-11614333
5	BHLHE40	chr8:11603932-11604097	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:11612814-11612989	K562	blood:	n/a	n/a
7	BHLHE40	chr8:11615028-11615339	K562	blood:	n/a	n/a
8	BRCA1	chr8:11608918-11608941	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr8:11614195-11614775	K562	blood:	n/a	n/a
10	CEBPB	chr8:11603846-11603972	IMR90	lung:	n/a	n/a
11	CEBPB	chr8:11608063-11608352	IMR90	lung:	n/a	n/a
12	CEBPB	chr8:11603802-11604061	K562	blood:	n/a	n/a
13	CEBPD	chr8:11614117-11614586	K562	blood:	n/a	n/a
14	CHD2	chr8:11613984-11614394	K562	blood:	n/a	n/a
15	CHD2	chr8:11603856-11604281	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr8:11604280-11604430	GM06990	blood:	n/a	n/a
17	CTCF	chr8:11603960-11604110	GM12874	blood:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11604017-11604033
18	CTCF	chr8:11612582-11612931	K562	blood:	n/a	chr8:11612738-11612751 chr8:11612738-11612747 chr8:11612735-11612753
19	CTCF	chr8:11612620-11612770	MCF-7	breast:	n/a	chr8:11612738-11612751 chr8:11612738-11612747 chr8:11612735-11612753
20	CTCF	chr8:11601562-11601640	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr8:11603960-11604110	HPAF	blood vessel:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11604017-11604033
22	CTCF	chr8:11603640-11603790	GM12867	blood:	n/a	n/a
23	CTCF	chr8:11612689-11612823	Fibrobl	skin:	n/a	chr8:11612738-11612751 chr8:11612738-11612747 chr8:11612735-11612753
24	CTCF	chr8:11601520-11601670	GM12866	blood:	n/a	n/a
25	CTCF	chr8:11603940-11604090	HUVEC	blood vessel:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11604017-11604033
26	CTCF	chr8:11603880-11604030	WI-38	lung:	n/a	chr8:11603922-11603929
27	CTCF	chr8:11603940-11604117	GM20000	blood:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11604017-11604033
28	CTCF	chr8:11616706-11616855	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:11612480-11612630	GM12871	blood:	n/a	n/a
30	CTCF	chr8:11603920-11604070	HFF	foreskin:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11603922-11603929 chr8:11604017-11604033
31	CTCF	chr8:11603960-11604110	AG09319	gingival:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11604017-11604033
32	CTCF	chr8:11603940-11604090	HepG2	liver:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11604017-11604033
33	CTCF	chr8:11603864-11604154	SK-N-SH_RA	brain:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11603922-11603929 chr8:11604017-11604033
34	CTCF	chr8:11603940-11604090	HRE	kidney:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11604017-11604033
35	CTCF	chr8:11604246-11604337	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:11603921-11604170	Pancreas_OC	pancreas:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11603922-11603929 chr8:11604017-11604033
37	CTCF	chr8:11603960-11604110	HA-sp	spinal cord:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11604017-11604033
38	CTCF	chr8:11603920-11604070	NHLF	lung:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11603922-11603929 chr8:11604017-11604033
39	CTCF	chr8:11603940-11604090	GM12865	blood:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11604017-11604033
40	CTCF	chr8:11603921-11604172	MCF-7	breast:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11603922-11603929 chr8:11604017-11604033
41	CTCF	chr8:11603879-11604176	GM19239	blood:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11603922-11603929 chr8:11604017-11604033
42	CTCF	chr8:11603743-11604283	MCF-7	breast:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11603922-11603929 chr8:11604017-11604033
43	CTCF	chr8:11616713-11616818	A549	lung:	n/a	n/a
44	CTCF	chr8:11612678-11612814	MCF-7	breast:	n/a	chr8:11612738-11612751 chr8:11612738-11612747 chr8:11612735-11612753
45	CTCF	chr8:11612660-11612810	HBMEC	blood vessel:	n/a	chr8:11612738-11612751 chr8:11612738-11612747 chr8:11612735-11612753
46	CTCF	chr8:11603867-11604163	A549	lung:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11603922-11603929 chr8:11604017-11604033
47	CTCF	chr8:11601540-11601690	GM12866	blood:	n/a	n/a
48	CTCF	chr8:11603960-11604110	HCPEpiC	choroid plexus:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11604017-11604033
49	CTCF	chr8:11604243-11604395	GM12892	blood:	n/a	n/a
50	CTCF	chr8:11603920-11604070	HRPEpiC	eye:	n/a	chr8:11604011-11604032 chr8:11604016-11604034 chr8:11603922-11603929 chr8:11604017-11604033

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11605722-11605772	HCM	heart:	n/a
2	chr8:11611189-11611239	HAEpiC	amniotic membrane:	n/a
3	chr8:11614472-11614522	IMR90	lung:	fetal
4	chr8:11605722-11605772	HCM	heart:	n/a
5	chr8:11611189-11611239	HAEpiC	amniotic membrane:	n/a
6	chr8:11614472-11614522	IMR90	lung:	fetal
7	chr8:11609706-11609756	NH-A	brain:	n/a
8	chr8:11616798-11616848	CMK	blood:	n/a
9	chr8:11605722-11605772	HPAEpiC	pulmonary alveolar:	n/a
10	chr8:11607386-11607436	HRE	kidney:	n/a
11	chr8:11614568-11614618	U87	brain:	n/a
12	chr8:11614568-11614618	K562	blood:	n/a
13	chr8:11611189-11611239	HL-60	blood:	n/a
14	chr8:11614568-11614618	T-47D	breast:	n/a
15	chr8:11614472-11614522	Jurkat	blood:	n/a
16	chr8:11609706-11609756	AG09309	skin:	n/a
17	chr8:11601603-11601653	LNCaP	prostate:	n/a
18	chr8:11616798-11616848	HRPEpiC	eye:	n/a
19	chr8:11616798-11616848	MCF-7	breast:	n/a
20	chr8:11607693-11607743	HCM	heart:	n/a
21	chr8:11611189-11611239	T-47D	breast:	n/a
22	chr8:11616798-11616848	HNPCEpiC	eye:	n/a
23	chr8:11605722-11605772	PrEC	prostate:	n/a
24	chr8:11604273-11604323	SK-N-MC	brain:	n/a
25	chr8:11614368-11614418	NH-A	brain:	n/a
26	chr8:11616798-11616848	A549	lung:	n/a
27	chr8:11614568-11614618	ECC-1	luminal epithelium:	n/a
28	chr8:11607693-11607743	GM06990	blood:	n/a
29	chr8:11614368-11614418	ovcar-3	ovarian:	n/a
30	chr8:11614568-11614618	GM12878	blood:	n/a
31	chr8:11607693-11607743	U87	brain:	n/a
32	chr8:11614368-11614418	GM06990	blood:	n/a
33	chr8:11614568-11614618	IMR90	lung:	fetal
34	chr8:11611189-11611239	NHDF-neo	bronchial:	n/a
35	chr8:11607693-11607743	LNCaP	prostate:	n/a
36	chr8:11614472-11614522	SAEC	small airway:	n/a
37	chr8:11605722-11605772	HRPEpiC	eye:	n/a
38	chr8:11614472-11614522	NT2-D1	testis:	n/a
39	chr8:11601603-11601653	AG09319	gingival:	n/a
40	chr8:11604273-11604323	RPTEC	kidney:	n/a
41	chr8:11611189-11611239	SAEC	small airway:	n/a
42	chr8:11614472-11614522	ovcar-3	ovarian:	n/a
43	chr8:11607557-11607607	ovcar-3	ovarian:	n/a
44	chr8:11604273-11604323	GM12891	blood:	n/a
45	chr8:11614568-11614618	AG09319	gingival:	n/a
46	chr8:11609706-11609756	AoSMC	blood vessel:	n/a
47	chr8:11607693-11607743	MCF-7	breast:	n/a
48	chr8:11614568-11614618	HCT-116	colon:	n/a
49	chr8:11616798-11616848	SKMC	muscle:	n/a
50	chr8:11607557-11607607	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:11420542..11422083-chr8:11608840..11610442,2	MCF-7	breast:
2	chr8:11587892..11588820-chr8:11603814..11604865,11	MCF-7	breast:
3	chr8:11573922..11574562-chr8:11603556..11604064,2	MCF-7	breast:
4	chr8:11604748..11607888-chr8:11608880..11611391,3	K562	blood:
5	chr8:11587887..11588889-chr8:11603840..11604789,8	MCF-7	breast:
6	chr8:11595827..11599047-chr8:11599477..11602717,3	K562	blood:
7	chr8:11614600..11617057-chr8:11621350..11623693,3	K562	blood:
8	chr8:11587278..11590197-chr8:11605996..11608000,2	MCF-7	breast:
9	chr8:11603020..11605526-chr8:11757590..11759777,2	K562	blood:
10	chr8:11594028..11596357-chr8:11603341..11605570,2	K562	blood:
11	chr8:11602490..11604038-chr8:11606565..11608594,2	K562	blood:
12	chr8:11612285..11613206-chr8:11801217..11801735,2	MCF-7	breast:
13	chr8:11614845..11616684-chr8:11618731..11620285,2	MCF-7	breast:
14	chr8:11604748..11607888-chr8:11608880..11611391,3	K562	blood:
15	chr8:11422237..11424811-chr8:11602615..11604781,2	MCF-7	breast:
16	chr8:11587850..11588855-chr8:11603787..11604777,28	MCF-7	breast:
17	chr8:11421842..11422772-chr8:11603355..11604431,7	MCF-7	breast:
18	chr8:11424667..11425261-chr8:11603180..11604185,3	MCF-7	breast:
19	chr8:11602490..11604038-chr8:11606565..11608594,2	K562	blood:
20	chr8:11430194..11430977-chr8:11603626..11604340,2	MCF-7	breast:
21	chr8:11446870..11447723-chr8:11603904..11604616,2	K562	blood:
22	chr8:11593617..11594422-chr8:11604399..11605223,2	K562	blood:
23	chr8:11422289..11424857-chr8:11598109..11600598,2	MCF-7	breast:
24	chr8:11421781..11422781-chr8:11603539..11604516,9	K562	blood:

Variant related genes	Relation type
GATA4	TF binding region
C8orf49	TF binding region
GATA4	CpG island
C8orf49	CpG island
ENSG00000255394	chromatin interactions

Extended variants
information (count: 966 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:966 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10090884	chr8:11599570-11599571	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556449590	chr8:11599585-11599586	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs577746627	chr8:11599613-11599614	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs375128546	chr8:11599658-11599659	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs545227698	chr8:11599678-11599679	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs66494852	chr8:11599681-11599682	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs76605420	chr8:11599685-11599686	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs7819212	chr8:11599741-11599742	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185832956	chr8:11599773-11599774	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs150188832	chr8:11599802-11599803	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs139156236	chr8:11599805-11599806	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs62489352	chr8:11599819-11599820	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs532595494	chr8:11599832-11599833	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs554374409	chr8:11599856-11599857	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs566149579	chr8:11599865-11599866	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs201647948	chr8:11599888-11599889	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs112876765	chr8:11599893-11599894	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs562905525	chr8:11599894-11599895	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs71521636	chr8:11599905-11599906	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs147633153	chr8:11599906-11599907	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs115673638	chr8:11599907-11599908	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs78077854	chr8:11599911-11599912	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs548687739	chr8:11599936-11599937	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs566900464	chr8:11599946-11599947	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs62489353	chr8:11599993-11599994	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs147512972	chr8:11599998-11599999	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs571563577	chr8:11600005-11600006	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs73539813	chr8:11600011-11600012	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs553898507	chr8:11600012-11600013	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs572292840	chr8:11600022-11600023	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
31	rs542750313	chr8:11600027-11600028	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
32	rs140126774	chr8:11600034-11600035	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
33	rs149613854	chr8:11600044-11600045	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
34	rs144407486	chr8:11600078-11600079	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
35	rs543846590	chr8:11600094-11600095	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs565137162	chr8:11600103-11600104	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs376628724	chr8:11600107-11600108	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs577423859	chr8:11600143-11600144	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs541373017	chr8:11600146-11600147	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs529668969	chr8:11600169-11600170	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
41	rs530258876	chr8:11600177-11600178	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
42	rs11785912	chr8:11600233-11600234	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs560689496	chr8:11600260-11600261	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
44	rs531203266	chr8:11600277-11600278	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
45	rs576062738	chr8:11600287-11600288	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
46	rs188734845	chr8:11600294-11600295	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
47	rs538897791	chr8:11600309-11600310	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
48	rs547403275	chr8:11600316-11600317	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
49	rs181118060	chr8:11600324-11600325	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs536494716	chr8:11600327-11600328	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Gastric cancer	22315472	CNVD
Gastric cancer	17229543	CNVD
Disorders of sex development	22290220	CNVD
Ependymoma	20639864	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11593400-11601400	Genic enhancers	Fetal Intestine Small	intestine
2	chr8:11595200-11600600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:11595400-11600600	Weak transcription	Colon Smooth Muscle	Colon
4	chr8:11596200-11604000	Enhancers	Pancreas	Pancrea
5	chr8:11597600-11600400	Enhancers	Right Ventricle	heart
6	chr8:11597600-11601000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr8:11597800-11599600	Enhancers	HepG2	liver
8	chr8:11597800-11600400	Enhancers	Gastric	stomach
9	chr8:11597800-11600600	Enhancers	Fetal Heart	heart
10	chr8:11598200-11600600	Enhancers	Placenta	Placenta
11	chr8:11598400-11604200	Enhancers	Stomach Mucosa	stomach
12	chr8:11598600-11600400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:11599000-11601000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr8:11599200-11599600	Flanking Active TSS	Liver	Liver
15	chr8:11599200-11599800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr8:11599200-11602000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:11599200-11602000	Flanking Active TSS	Ovary	ovary
18	chr8:11599200-11602400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
19	chr8:11599200-11602600	Enhancers	Duodenum Mucosa	Duodenum
20	chr8:11599200-11605000	Enhancers	Left Ventricle	heart
21	chr8:11599400-11599600	Bivalent Enhancer	Fetal Intestine Large	intestine
22	chr8:11599400-11599600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
23	chr8:11599400-11599800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:11599400-11601000	Enhancers	Right Atrium	heart
25	chr8:11599400-11602000	Bivalent Enhancer	Fetal Stomach	stomach
26	chr8:11599400-11602000	Enhancers	Rectal Smooth Muscle	rectum
27	chr8:11599600-11600000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
28	chr8:11599600-11600200	Genic enhancers	HepG2	liver
29	chr8:11599600-11600400	Enhancers	Liver	Liver
30	chr8:11599600-11600600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr8:11599800-11600000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr8:11599800-11600000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
33	chr8:11599800-11600200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:11599800-11600800	Enhancers	Placenta Amnion	Placenta Amnion
35	chr8:11600000-11600200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
36	chr8:11600000-11600200	Bivalent Enhancer	Fetal Muscle Leg	muscle
37	chr8:11600000-11600400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr8:11600000-11600600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:11600000-11600600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
40	chr8:11600200-11600400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr8:11600200-11600400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr8:11600200-11600600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
43	chr8:11600200-11600600	Bivalent Enhancer	Fetal Intestine Large	intestine
44	chr8:11600200-11601200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr8:11600200-11602000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:11600200-11602200	Enhancers	HepG2	liver
47	chr8:11600200-11602400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr8:11600400-11600600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr8:11600400-11601000	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:11600400-11601200	Flanking Active TSS	Liver	Liver

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