Variant report

Variant	nsv1040359
Chromosome Location	chr10:43562033-43591617
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	BHLHE40	chr10:43574476-43574611	K562	blood:	n/a	n/a
2	BHLHE40	chr10:43574377-43574555	HepG2	liver:	n/a	n/a
3	BRCA1	chr10:43574519-43574717	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr10:43574341-43574661	K562	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
5	CTCF	chr10:43574431-43574670	LNCaP	prostate:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
6	CTCF	chr10:43571040-43571190	HMEC	breast:	n/a	n/a
7	CTCF	chr10:43574480-43574630	SK-N-SH_RA	brain:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
8	CTCF	chr10:43574434-43574695	NHEK	skin:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
9	CTCF	chr10:43571900-43572050	SK-N-SH_RA	brain:	n/a	chr10:43571958-43571971 chr10:43571942-43571955
10	CTCF	chr10:43574411-43574716	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
11	CTCF	chr10:43571046-43571212	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr10:43566240-43566390	K562	blood:	n/a	n/a
13	CTCF	chr10:43588920-43589070	HFF-Myc	foreskin:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
14	CTCF	chr10:43571026-43571234	LNCaP	prostate:	n/a	n/a
15	CTCF	chr10:43571011-43571322	MCF-7	breast:	n/a	n/a
16	CTCF	chr10:43571080-43571230	HA-sp	spinal cord:	n/a	n/a
17	CTCF	chr10:43574480-43574630	GM12869	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
18	CTCF	chr10:43574500-43574650	GM12865	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
19	CTCF	chr10:43571060-43571201	GM12892	blood:	n/a	n/a
20	CTCF	chr10:43574060-43574210	GM12865	blood:	n/a	n/a
21	CTCF	chr10:43574480-43574630	HVMF	connective:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
22	CTCF	chr10:43574520-43574670	GM12871	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
23	CTCF	chr10:43571020-43571170	RPTEC	kidney:	n/a	n/a
24	CTCF	chr10:43574414-43574709	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
25	CTCF	chr10:43572553-43572602	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr10:43571065-43571191	HepG2	liver:	n/a	n/a
27	CTCF	chr10:43566262-43566367	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr10:43574444-43574649	Spleen_OC	spleen:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
29	CTCF	chr10:43574343-43574713	T-47D	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
30	CTCF	chr10:43574447-43574648	GM10266	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
31	CTCF	chr10:43574423-43574701	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
32	CTCF	chr10:43571898-43572035	NHEK	skin:	n/a	chr10:43571958-43571971 chr10:43571942-43571955
33	CTCF	chr10:43574500-43574650	NHEK	skin:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
34	CTCF	chr10:43571063-43571180	GM19240	blood:	n/a	n/a
35	CTCF	chr10:43565240-43565390	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr10:43571060-43571185	GM13977	blood:	n/a	n/a
37	CTCF	chr10:43571060-43571210	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr10:43574352-43574772	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
39	CTCF	chr10:43570993-43571330	K562	blood:	n/a	n/a
40	CTCF	chr10:43572480-43572630	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr10:43571028-43571340	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:43574480-43574630	GM12873	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
43	CTCF	chr10:43571040-43571190	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr10:43574440-43574590	GM12868	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
45	CTCF	chr10:43588960-43589110	HA-sp	spinal cord:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
46	CTCF	chr10:43571058-43571062	GM19240	blood:	n/a	n/a
47	CTCF	chr10:43574460-43574610	HA-sp	spinal cord:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
48	CTCF	chr10:43588940-43589090	AG04449	skin:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
49	CTCF	chr10:43571080-43571230	HCM	heart:	n/a	n/a
50	CTCF	chr10:43574383-43574666	H1-hESC	embryonic stem cell:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43572430-43572480	HNPCEpiC	eye:	n/a
2	chr10:43572430-43572480	HNPCEpiC	eye:	n/a
3	chr10:43573195-43573245	GM12878	blood:	n/a
4	chr10:43572621-43572671	Hepatocyte	liver:	n/a
5	chr10:43585188-43585238	CMK	blood:	n/a
6	chr10:43571169-43571219	HepG2	liver:	n/a
7	chr10:43572065-43572115	Hepatocyte	liver:	n/a
8	chr10:43569045-43569095	LNCaP	prostate:	n/a
9	chr10:43569045-43569095	K562	blood:	n/a
10	chr10:43572621-43572671	GM12892	blood:	n/a
11	chr10:43562813-43562863	GM12878	blood:	n/a
12	chr10:43572467-43572517	HMEC	breast:	n/a
13	chr10:43569045-43569095	HRPEpiC	eye:	n/a
14	chr10:43572065-43572115	Hela-S3	cervix:	n/a
15	chr10:43573332-43573382	GM06990	blood:	n/a
16	chr10:43572413-43572463	Hepatocyte	liver:	n/a
17	chr10:43572430-43572480	SK-N-SH_RA	brain:	n/a
18	chr10:43573195-43573245	HCPEpiC	choroid plexus:	n/a
19	chr10:43572467-43572517	HL-60	blood:	n/a
20	chr10:43572795-43572845	HCT-116	colon:	n/a
21	chr10:43572467-43572517	HCT-116	colon:	n/a
22	chr10:43569045-43569095	HCM	heart:	n/a
23	chr10:43572065-43572115	HepG2	liver:	n/a
24	chr10:43572795-43572845	HNPCEpiC	eye:	n/a
25	chr10:43572621-43572671	SKMC	muscle:	n/a
26	chr10:43572621-43572671	AG04449	skin:	fetal
27	chr10:43573195-43573245	HCF	heart:	n/a
28	chr10:43572467-43572517	HCM	heart:	n/a
29	chr10:43573195-43573245	HIPEpiC	eye:	n/a
30	chr10:43577025-43577075	HepG2	liver:	n/a
31	chr10:43572413-43572463	NT2-D1	testis:	n/a
32	chr10:43575142-43575192	HRPEpiC	eye:	n/a
33	chr10:43562813-43562863	HCM	heart:	n/a
34	chr10:43572430-43572480	HIPEpiC	eye:	n/a
35	chr10:43585188-43585238	HEEpiC	esophagus:	n/a
36	chr10:43571169-43571219	HCT-116	colon:	n/a
37	chr10:43572413-43572463	HL-60	blood:	n/a
38	chr10:43575142-43575192	SK-N-SH	brain:	n/a
39	chr10:43571169-43571219	AG10803	skin:	n/a
40	chr10:43577025-43577075	GM06990	blood:	n/a
41	chr10:43572621-43572671	HepG2	liver:	n/a
42	chr10:43573332-43573382	MCF-7	breast:	n/a
43	chr10:43573319-43573369	HCT-116	colon:	n/a
44	chr10:43572467-43572517	IMR90	lung:	fetal
45	chr10:43572621-43572671	HCPEpiC	choroid plexus:	n/a
46	chr10:43575142-43575192	PANC-1	pancreas:	n/a
47	chr10:43569045-43569095	CMK	blood:	n/a
48	chr10:43569045-43569095	AG10803	skin:	n/a
49	chr10:43572424-43572474	H1-hESC	embryonic stem cell:	embryo
50	chr10:43569045-43569095	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43496061..43498951-chr10:43575386..43576961,2	MCF-7	breast:
2	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
3	chr10:43585387..43587338-chr10:43587452..43589523,2	K562	blood:
4	chr10:43520913..43524676-chr10:43563115..43566179,5	MCF-7	breast:
5	chr10:43557710..43559940-chr10:43561579..43563313,2	K562	blood:
6	chr10:43562026..43563048-chr17:73389362..73390234,5	MCF-7	breast:
7	chr10:43561322..43565766-chr10:43567124..43571353,6	K562	blood:
8	chr10:43583134..43585872-chr10:43588187..43591197,3	MCF-7	breast:
9	chr10:43583134..43585872-chr10:43588187..43591197,3	MCF-7	breast:
10	chr10:43470988..43471723-chr10:43574194..43574824,2	MCF-7	breast:
11	chr10:43561623..43563408-chr10:43565036..43569380,4	MCF-7	breast:
12	chr10:43567330..43568843-chr10:43570636..43572926,2	MCF-7	breast:
13	chr10:43521597..43522422-chr10:43563847..43564424,2	MCF-7	breast:
14	chr10:43370478..43372425-chr10:43586111..43588010,2	MCF-7	breast:
15	chr10:43561623..43563408-chr10:43565036..43569380,4	MCF-7	breast:
16	chr10:43521600..43522503-chr10:43589625..43590206,2	MCF-7	breast:
17	chr10:43561322..43565766-chr10:43567124..43571353,6	K562	blood:
18	chr10:43563253..43566538-chr10:43567124..43569938,3	K562	blood:
19	chr10:43589175..43591364-chr10:43599200..43601057,2	MCF-7	breast:
20	chr10:43576417..43579207-chr10:43590495..43592572,2	MCF-7	breast:
21	chr10:43520346..43523029-chr10:43587909..43590894,3	MCF-7	breast:
22	chr10:43589023..43591875-chr10:43596909..43598786,2	MCF-7	breast:
23	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
24	chr10:43516622..43519495-chr10:43560494..43562660,2	MCF-7	breast:
25	chr10:43571954..43575948-chr10:43588456..43593172,4	MCF-7	breast:
26	chr10:43521523..43522449-chr10:43577293..43578240,8	MCF-7	breast:
27	chr10:43588801..43589617-chr10:43600178..43601154,2	MCF-7	breast:
28	chr10:43322775..43323340-chr10:43574006..43574597,2	MCF-7	breast:
29	chr10:43576417..43579207-chr10:43590495..43592572,2	MCF-7	breast:
30	chr10:43563253..43566538-chr10:43567124..43569938,3	K562	blood:
31	chr10:43577015..43578995-chr10:43604341..43606597,2	MCF-7	breast:
32	chr10:43476676..43477639-chr10:43581673..43582410,2	MCF-7	breast:
33	chr10:43579643..43581967-chr10:43583481..43585726,2	MCF-7	breast:
34	chr10:43578754..43580371-chr10:43586605..43589212,2	MCF-7	breast:
35	chr10:43553627..43556215-chr10:43562865..43565687,3	MCF-7	breast:
36	chr10:43361782..43362789-chr10:43574108..43574983,3	K562	blood:
37	chr10:43578198..43579973-chr10:43594655..43597408,2	MCF-7	breast:
38	chr10:43588758..43591392-chr10:43592644..43594640,2	MCF-7	breast:
39	chr10:43576471..43578600-chr10:43587847..43590261,2	MCF-7	breast:
40	chr10:43362412..43363000-chr10:43573894..43574641,2	MCF-7	breast:
41	chr10:43587904..43589717-chr10:43600959..43603478,2	MCF-7	breast:
42	chr10:43571757..43578165-chr10:43578692..43585292,10	MCF-7	breast:
43	chr10:43563405..43565262-chr10:43578421..43580080,2	K562	blood:
44	chr10:43579643..43581967-chr10:43583481..43585726,2	MCF-7	breast:
45	chr10:43563405..43565262-chr10:43578421..43580080,2	K562	blood:
46	chr10:43556494..43558733-chr10:43559960..43563613,3	MCF-7	breast:
47	chr10:43361921..43363073-chr10:43574052..43574909,5	MCF-7	breast:
48	chr10:43521611..43522326-chr10:43577256..43578049,6	MCF-7	breast:
49	chr10:43589765..43592695-chr10:43600961..43603100,2	MCF-7	breast:
50	chr10:43572567..43574576-chr10:43871912..43874300,2	MCF-7	breast:

Variant related genes	Relation type
RET	TF binding region
RET	CpG island
ENSG00000229630	chromatin interactions
ENSG00000265342	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000177885	chromatin interactions
ENSG00000273008	chromatin interactions
ENSG00000234944	chromatin interactions
ENSG00000169826	chromatin interactions

Extended variants
information (count: 1147 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1147 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2435369	chr10:43562108-43562109	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566677585	chr10:43562156-43562157	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs144619018	chr10:43562158-43562159	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs372623249	chr10:43562159-43562160	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs570814699	chr10:43562264-43562265	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs538381213	chr10:43562322-43562323	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs3026712	chr10:43562337-43562338	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2505988	chr10:43562340-43562341	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs3026713	chr10:43562479-43562480	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs542077380	chr10:43562497-43562498	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs61024707	chr10:43562536-43562537	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs554154380	chr10:43562538-43562539	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs572414636	chr10:43562542-43562543	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546039431	chr10:43562544-43562545	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs564583634	chr10:43562545-43562546	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs3026714	chr10:43562593-43562594	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186183043	chr10:43562617-43562618	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs562422359	chr10:43562618-43562619	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs148479387	chr10:43562641-43562642	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141441272	chr10:43562740-43562741	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560349964	chr10:43562758-43562759	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs535711702	chr10:43562759-43562760	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs191046521	chr10:43562774-43562775	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs182800516	chr10:43562784-43562785	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs570889797	chr10:43562802-43562803	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs73266104	chr10:43562845-43562846	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs187450411	chr10:43562853-43562854	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs568475871	chr10:43562884-43562885	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs535900721	chr10:43562903-43562904	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs554075241	chr10:43562910-43562911	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs115769984	chr10:43562997-43562998	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs539785022	chr10:43563025-43563026	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs558013620	chr10:43563035-43563036	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs114984462	chr10:43563058-43563059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192340187	chr10:43563168-43563169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139644677	chr10:43563175-43563176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs71505660	chr10:43563176-43563177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541865834	chr10:43563177-43563178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575523250	chr10:43563192-43563193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs3026716	chr10:43563260-43563261	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs527464801	chr10:43563295-43563296	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs552524833	chr10:43563297-43563298	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs564392717	chr10:43563321-43563322	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs3026717	chr10:43563326-43563327	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs113429168	chr10:43563330-43563331	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs2435368	chr10:43563348-43563349	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs3026719	chr10:43563367-43563368	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs535621100	chr10:43563389-43563390	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs540425585	chr10:43563407-43563408	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs547476516	chr10:43563411-43563412	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43554400-43572000	Weak transcription	Right Atrium	heart
2	chr10:43556800-43563200	Weak transcription	Spleen	Spleen
3	chr10:43558000-43563400	Weak transcription	Right Ventricle	heart
4	chr10:43559000-43562600	Weak transcription	Esophagus	oesophagus
5	chr10:43560000-43564400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr10:43560800-43570800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr10:43561600-43565200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:43561800-43563000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:43561800-43563600	Weak transcription	Fetal Muscle Leg	muscle
10	chr10:43562600-43562800	Enhancers	Esophagus	oesophagus
11	chr10:43562800-43564600	Enhancers	Adipose Nuclei	Adipose
12	chr10:43562800-43571800	Weak transcription	Esophagus	oesophagus
13	chr10:43563000-43572000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr10:43563200-43565800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr10:43563400-43563600	Enhancers	Right Ventricle	heart
16	chr10:43563400-43563600	Enhancers	Spleen	Spleen
17	chr10:43563400-43565600	Bivalent Enhancer	Fetal Stomach	stomach
18	chr10:43563600-43564200	Enhancers	Fetal Muscle Leg	muscle
19	chr10:43564000-43564200	Enhancers	Colon Smooth Muscle	Colon
20	chr10:43564000-43564200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr10:43564200-43564600	Flanking Active TSS	Colon Smooth Muscle	Colon
22	chr10:43564200-43564600	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr10:43564200-43564600	Enhancers	Placenta	Placenta
24	chr10:43564200-43565000	Bivalent Enhancer	Fetal Muscle Leg	muscle
25	chr10:43564400-43564600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr10:43564400-43565000	Enhancers	Rectal Smooth Muscle	rectum
27	chr10:43564600-43565000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr10:43564600-43565000	Bivalent Enhancer	Placenta	Placenta
29	chr10:43564600-43565200	Enhancers	Fetal Kidney	kidney
30	chr10:43564600-43565600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr10:43565000-43565400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr10:43565000-43565600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr10:43565200-43566600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr10:43565600-43566600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr10:43566200-43566400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr10:43566600-43570200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr10:43570200-43571400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr10:43570400-43570600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr10:43570400-43570800	Bivalent Enhancer	Fetal Stomach	stomach
40	chr10:43570600-43570800	Bivalent Enhancer	Right Ventricle	heart
41	chr10:43570600-43570800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
42	chr10:43570800-43571200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr10:43571000-43572000	Bivalent Enhancer	Fetal Stomach	stomach
44	chr10:43571200-43571400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
45	chr10:43571200-43571400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr10:43571200-43571400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
47	chr10:43571200-43571400	Bivalent/Poised TSS	Spleen	Spleen
48	chr10:43571200-43571400	Enhancers	A549	lung
49	chr10:43571200-43571800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:43571200-43572000	Bivalent Enhancer	Colonic Mucosa	Colon

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