Variant report

Variant	nsv1050241
Chromosome Location	chr10:43562033-43592346
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	chr10:43588980-43589130	AG09319	gingival:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
5	CTCF	chr10:43566220-43566370	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr10:43574417-43574728	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
7	CTCF	chr10:43571020-43571170	BE2_C	brain:	n/a	n/a
8	CTCF	chr10:43574448-43574656	Hela-S3	cervix:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
9	CTCF	chr10:43574480-43574630	GM12873	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
10	CTCF	chr10:43571040-43571190	GM12870	blood:	n/a	n/a
11	CTCF	chr10:43588915-43589161	MCF-7	breast:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
12	CTCF	chr10:43566127-43566404	K562	blood:	n/a	n/a
13	CTCF	chr10:43571040-43571190	GM12875	blood:	n/a	n/a
14	CTCF	chr10:43574351-43574722	K562	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
15	CTCF	chr10:43571900-43572050	BJ	skin:	n/a	chr10:43571958-43571971 chr10:43571942-43571955
16	CTCF	chr10:43571000-43571150	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr10:43566200-43566350	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr10:43588980-43589130	HEEpiC	esophagus:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
19	CTCF	chr10:43571020-43571170	K562	blood:	n/a	n/a
20	CTCF	chr10:43588940-43589090	Hela-S3	cervix:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
21	CTCF	chr10:43574500-43574650	GM12864	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
22	CTCF	chr10:43588940-43589090	AG04449	skin:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
23	CTCF	chr10:43588940-43589090	HRPEpiC	eye:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
24	CTCF	chr10:43571040-43571190	GM12864	blood:	n/a	n/a
25	CTCF	chr10:43574414-43574709	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
26	CTCF	chr10:43588940-43589090	HEEpiC	esophagus:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
27	CTCF	chr10:43571000-43571150	HPF	lung:	n/a	n/a
28	CTCF	chr10:43588782-43589153	T-47D	breast:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
29	CTCF	chr10:43571080-43571230	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr10:43571040-43571190	AG09319	gingival:	n/a	n/a
31	CTCF	chr10:43589047-43589050	GM10248	blood:	n/a	n/a
32	CTCF	chr10:43574460-43574610	GM06990	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
33	CTCF	chr10:43574463-43574613	A549	lung:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
34	CTCF	chr10:43574460-43574610	AoAF	blood vessel:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
35	CTCF	chr10:43588920-43589070	Caco-2	colon:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
36	CTCF	chr10:43588940-43589090	HMF	breast:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
37	CTCF	chr10:43571060-43571210	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr10:43571078-43571183	ProgFib	skin:	n/a	n/a
39	CTCF	chr10:43574560-43574710	K562	blood:	n/a	n/a
40	CTCF	chr10:43571043-43571207	GM12878	blood:	n/a	n/a
41	CTCF	chr10:43571900-43572050	Caco-2	colon:	n/a	chr10:43571958-43571971 chr10:43571942-43571955
42	CTCF	chr10:43588986-43589073	GM10266	blood:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
43	CTCF	chr10:43571026-43571234	LNCaP	prostate:	n/a	n/a
44	CTCF	chr10:43571060-43571210	Caco-2	colon:	n/a	n/a
45	CTCF	chr10:43571080-43571230	GM12866	blood:	n/a	n/a
46	CTCF	chr10:43566124-43566410	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr10:43571840-43571990	A549	lung:	n/a	chr10:43571958-43571971 chr10:43571942-43571955
48	CTCF	chr10:43566140-43566290	HepG2	liver:	n/a	n/a
49	CTCF	chr10:43566500-43566650	NB4	blood:	n/a	n/a
50	CTCF	chr10:43588932-43589144	LNCaP	prostate:	n/a	chr10:43589022-43589043 chr10:43589027-43589045

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43572621-43572671	HPAEpiC	pulmonary alveolar:	n/a
2	chr10:43573195-43573245	HRE	kidney:	n/a
3	chr10:43575142-43575192	PrEC	prostate:	n/a
4	chr10:43572359-43572409	BJ	skin:	n/a
5	chr10:43572621-43572671	SAEC	small airway:	n/a
6	chr10:43573195-43573245	NB4	blood:	n/a
7	chr10:43575142-43575192	AG09309	skin:	n/a
8	chr10:43585188-43585238	NHBE	bronchial:	n/a
9	chr10:43562813-43562863	HUVEC	blood vessel:	n/a
10	chr10:43562813-43562863	ovcar-3	ovarian:	n/a
11	chr10:43572424-43572474	RPTEC	kidney:	n/a
12	chr10:43573332-43573382	NT2-D1	testis:	n/a
13	chr10:43577025-43577075	HCT-116	colon:	n/a
14	chr10:43562813-43562863	PrEC	prostate:	n/a
15	chr10:43572244-43572294	NT2-D1	testis:	n/a
16	chr10:43572795-43572845	A549	lung:	n/a
17	chr10:43572065-43572115	U87	brain:	n/a
18	chr10:43573195-43573245	NHDF-neo	bronchial:	n/a
19	chr10:43572065-43572115	GM06990	blood:	n/a
20	chr10:43573195-43573245	NH-A	brain:	n/a
21	chr10:43572065-43572115	Hela-S3	cervix:	n/a
22	chr10:43573319-43573369	HCM	heart:	n/a
23	chr10:43585188-43585238	AG04449	skin:	fetal
24	chr10:43571169-43571219	HCT-116	colon:	n/a
25	chr10:43572795-43572845	U87	brain:	n/a
26	chr10:43571169-43571219	SK-N-MC	brain:	n/a
27	chr10:43575142-43575192	GM12878	blood:	n/a
28	chr10:43572413-43572463	MCF10A-Er-Src	breast:	n/a
29	chr10:43573195-43573245	HAEpiC	amniotic membrane:	n/a
30	chr10:43572795-43572845	SAEC	small airway:	n/a
31	chr10:43577025-43577075	HAEpiC	amniotic membrane:	n/a
32	chr10:43562544-43562594	SK-N-SH_RA	brain:	n/a
33	chr10:43572621-43572671	K562	blood:	n/a
34	chr10:43573332-43573382	HCM	heart:	n/a
35	chr10:43572244-43572294	AG10803	skin:	n/a
36	chr10:43572424-43572474	AG04450	lung:	fetal
37	chr10:43572065-43572115	SK-N-SH	brain:	n/a
38	chr10:43562544-43562594	Hepatocyte	liver:	n/a
39	chr10:43573319-43573369	HL-60	blood:	n/a
40	chr10:43569045-43569095	K562	blood:	n/a
41	chr10:43572065-43572115	Caco-2	colon:	n/a
42	chr10:43572065-43572115	NH-A	brain:	n/a
43	chr10:43572430-43572480	ovcar-3	ovarian:	n/a
44	chr10:43572065-43572115	SK-N-MC	brain:	n/a
45	chr10:43575142-43575192	GM12891	blood:	n/a
46	chr10:43577025-43577075	PFSK-1	brain:	n/a
47	chr10:43572621-43572671	Jurkat	blood:	n/a
48	chr10:43572621-43572671	LNCaP	prostate:	n/a
49	chr10:43575142-43575192	HEK293	kidney:	embryo
50	chr10:43572424-43572474	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43521899..43522422-chr10:43563847..43564568,2	MCF-7	breast:
2	chr10:43563405..43565262-chr10:43578421..43580080,2	K562	blood:
3	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
4	chr10:43523482..43525302-chr10:43587306..43589145,2	MCF-7	breast:
5	chr10:43517701..43518324-chr10:43573585..43574127,2	MCF-7	breast:
6	chr10:43578754..43580371-chr10:43586605..43589212,2	MCF-7	breast:
7	chr10:43563253..43566538-chr10:43567124..43569938,3	K562	blood:
8	chr10:43322775..43323340-chr10:43574006..43574597,2	MCF-7	breast:
9	chr10:43521523..43522449-chr10:43577293..43578240,8	MCF-7	breast:
10	chr10:43557710..43559940-chr10:43561579..43563313,2	K562	blood:
11	chr10:43583134..43585872-chr10:43588187..43591197,3	MCF-7	breast:
12	chr10:43579643..43581967-chr10:43583481..43585726,2	MCF-7	breast:
13	chr10:43571757..43578165-chr10:43578692..43585292,10	MCF-7	breast:
14	chr10:43522095..43524147-chr10:43592185..43594122,2	MCF-7	breast:
15	chr10:43521597..43522422-chr10:43563847..43564424,2	MCF-7	breast:
16	chr10:43567330..43568843-chr10:43570636..43572926,2	MCF-7	breast:
17	chr10:43564728..43567195-chr10:43570638..43572674,3	MCF-7	breast:
18	chr10:43563405..43565262-chr10:43578421..43580080,2	K562	blood:
19	chr10:43574441..43574987-chr10:43601035..43601611,2	K562	blood:
20	chr10:43562048..43563046-chr17:73389829..73390578,3	MCF-7	breast:
21	chr10:43520346..43523029-chr10:43587909..43590894,3	MCF-7	breast:
22	chr10:43521600..43522503-chr10:43589625..43590206,2	MCF-7	breast:
23	chr10:43588801..43589617-chr10:43600178..43601154,2	MCF-7	breast:
24	chr10:43589175..43591364-chr10:43599200..43601057,2	MCF-7	breast:
25	chr10:43563253..43566538-chr10:43567124..43569938,3	K562	blood:
26	chr10:43587904..43589717-chr10:43600959..43603478,2	MCF-7	breast:
27	chr10:43576471..43578600-chr10:43587847..43590261,2	MCF-7	breast:
28	chr10:43521617..43522540-chr10:43581453..43582423,6	MCF-7	breast:
29	chr10:43578754..43580371-chr10:43586605..43589212,2	MCF-7	breast:
30	chr10:43589023..43591875-chr10:43596909..43598786,2	MCF-7	breast:
31	chr10:43363801..43367756-chr10:43571423..43575718,4	MCF-7	breast:
32	chr10:43576417..43579207-chr10:43590495..43592572,2	MCF-7	breast:
33	chr10:43561322..43565766-chr10:43567124..43571353,6	K562	blood:
34	chr10:43496061..43498951-chr10:43575386..43576961,2	MCF-7	breast:
35	chr10:43572567..43574576-chr10:43871912..43874300,2	MCF-7	breast:
36	chr10:43585387..43587338-chr10:43587452..43589523,2	K562	blood:
37	chr10:43476676..43477639-chr10:43581673..43582410,2	MCF-7	breast:
38	chr10:43576417..43579207-chr10:43590495..43592572,2	MCF-7	breast:
39	chr10:43578198..43579973-chr10:43594655..43597408,2	MCF-7	breast:
40	chr10:43577015..43578995-chr10:43604341..43606597,2	MCF-7	breast:
41	chr10:43574755..43578524-chr10:43632183..43633949,3	MCF-7	breast:
42	chr10:43561623..43563408-chr10:43565036..43569380,4	MCF-7	breast:
43	chr10:43588758..43591392-chr10:43592644..43594640,2	MCF-7	breast:
44	chr10:43470988..43471723-chr10:43574194..43574824,2	MCF-7	breast:
45	chr10:43521611..43522326-chr10:43577256..43578049,6	MCF-7	breast:
46	chr10:43362412..43363000-chr10:43573894..43574641,2	MCF-7	breast:
47	chr10:43370478..43372425-chr10:43586111..43588010,2	MCF-7	breast:
48	chr10:43516622..43519495-chr10:43560494..43562660,2	MCF-7	breast:
49	chr10:43361921..43363073-chr10:43574052..43574909,5	MCF-7	breast:
50	chr10:43553627..43556215-chr10:43562865..43565687,3	MCF-7	breast:

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

Extended variants
information (count: 1169 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1169 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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:527 , 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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