Variant report

Variant	nsv522566
Chromosome Location	chr10:43596728-43610671
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:621)
CpG islands
(count:978)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:621 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43601076-43601148	K562	blood:	n/a	n/a
2	ARID3A	chr10:43601022-43601255	HepG2	liver:	n/a	n/a
3	ATF2	chr10:43600926-43601267	GM12878	blood:	n/a	n/a
4	ATF3	chr10:43605779-43605949	K562	blood:	n/a	chr10:43605892-43605901
5	ATF3	chr10:43605769-43605874	GM12878	blood:	n/a	n/a
6	ATF3	chr10:43605698-43605963	GM12878	blood:	n/a	chr10:43605892-43605901
7	BACH1	chr10:43598601-43598610	K562	blood:	n/a	n/a
8	BACH1	chr10:43600017-43601367	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:43601044-43601195	K562	blood:	n/a	n/a
10	BHLHE40	chr10:43600953-43601265	K562	blood:	n/a	chr10:43601124-43601140 chr10:43601094-43601110
11	BHLHE40	chr10:43600562-43601406	GM12878	blood:	n/a	chr10:43601124-43601140 chr10:43601094-43601110
12	BHLHE40	chr10:43605688-43606015	K562	blood:	n/a	n/a
13	BHLHE40	chr10:43605670-43606046	GM12878	blood:	n/a	n/a
14	BHLHE40	chr10:43604992-43605096	K562	blood:	n/a	n/a
15	BRCA1	chr10:43600927-43601099	GM12878	blood:	n/a	n/a
16	BRCA1	chr10:43600998-43601231	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr10:43600940-43601262	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr10:43600966-43601106	HepG2	liver:	n/a	n/a
19	CBX3	chr10:43600952-43601300	K562	blood:	n/a	n/a
20	CCNT2	chr10:43600864-43601219	K562	blood:	n/a	n/a
21	CEBPB	chr10:43608753-43608944	HepG2	liver:	n/a	n/a
22	CEBPB	chr10:43600978-43601161	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr10:43608823-43608934	IMR90	lung:	n/a	n/a
24	CEBPD	chr10:43600916-43601277	HepG2	liver:	n/a	n/a
25	CHD1	chr10:43600781-43600967	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr10:43601069-43601208	HepG2	liver:	n/a	n/a
27	CHD2	chr10:43600617-43601308	GM12878	blood:	n/a	n/a
28	CHD2	chr10:43601007-43601377	K562	blood:	n/a	n/a
29	CHD2	chr10:43600094-43601220	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr10:43600949-43601228	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr10:43600858-43601262	A549	lung:	n/a	n/a
32	CTBP2	chr10:43600199-43601295	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr10:43608620-43608770	AG09309	skin:	n/a	n/a
34	CTCF	chr10:43601060-43601210	NB4	blood:	n/a	chr10:43601098-43601111 chr10:43601091-43601112 chr10:43601139-43601148 chr10:43601096-43601114 chr10:43601103-43601111
35	CTCF	chr10:43600825-43601229	A549	lung:	n/a	chr10:43601098-43601111 chr10:43601091-43601112 chr10:43601139-43601148 chr10:43601096-43601114 chr10:43601103-43601111
36	CTCF	chr10:43601060-43601210	BE2_C	brain:	n/a	chr10:43601098-43601111 chr10:43601091-43601112 chr10:43601139-43601148 chr10:43601096-43601114 chr10:43601103-43601111
37	CTCF	chr10:43600940-43601090	HAc	cerebellar:	n/a	n/a
38	CTCF	chr10:43600942-43601246	HepG2	liver:	n/a	chr10:43601098-43601111 chr10:43601091-43601112 chr10:43601139-43601148 chr10:43601096-43601114 chr10:43601103-43601111
39	CTCF	chr10:43600666-43601562	A549	lung:	n/a	chr10:43601098-43601111 chr10:43601091-43601112 chr10:43601139-43601148 chr10:43601096-43601114 chr10:43601103-43601111
40	CTCF	chr10:43605820-43605970	HCM	heart:	n/a	n/a
41	CTCF	chr10:43597420-43597570	GM12875	blood:	n/a	n/a
42	CTCF	chr10:43601040-43601190	HMEC	breast:	n/a	chr10:43601098-43601111 chr10:43601091-43601112 chr10:43601139-43601148 chr10:43601096-43601114 chr10:43601103-43601111
43	CTCF	chr10:43601440-43601590	HFF	foreskin:	n/a	n/a
44	CTCF	chr10:43605220-43605370	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr10:43600955-43601301	Fibrobl	skin:	n/a	chr10:43601098-43601111 chr10:43601091-43601112 chr10:43601139-43601148 chr10:43601096-43601114 chr10:43601103-43601111
46	CTCF	chr10:43601100-43601250	WI-38	lung:	n/a	chr10:43601139-43601148 chr10:43601103-43601111
47	CTCF	chr10:43601060-43601210	GM12865	blood:	n/a	chr10:43601098-43601111 chr10:43601091-43601112 chr10:43601139-43601148 chr10:43601096-43601114 chr10:43601103-43601111
48	CTCF	chr10:43609020-43609170	GM12869	blood:	n/a	n/a
49	CTCF	chr10:43605920-43606070	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr10:43601369-43601420	GM12878	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43603918-43603968	Hela-S3	cervix:	n/a
2	chr10:43603067-43603117	NT2-D1	testis:	n/a
3	chr10:43603918-43603968	Hela-S3	cervix:	n/a
4	chr10:43603067-43603117	NT2-D1	testis:	n/a
5	chr10:43600239-43600289	NHDF-neo	bronchial:	n/a
6	chr10:43599566-43599616	Jurkat	blood:	n/a
7	chr10:43599476-43599526	HCF	heart:	n/a
8	chr10:43601862-43601912	NHDF-neo	bronchial:	n/a
9	chr10:43600497-43600547	MCF10A-Er-Src	breast:	n/a
10	chr10:43603918-43603968	U87	brain:	n/a
11	chr10:43598772-43598822	GM12891	blood:	n/a
12	chr10:43603918-43603968	MCF-7	breast:	n/a
13	chr10:43600497-43600547	HCF	heart:	n/a
14	chr10:43599563-43599613	GM06990	blood:	n/a
15	chr10:43605906-43605956	A549	lung:	n/a
16	chr10:43601916-43601966	MCF-7	breast:	n/a
17	chr10:43600706-43600756	K562	blood:	n/a
18	chr10:43599563-43599613	HL-60	blood:	n/a
19	chr10:43599563-43599613	A549	lung:	n/a
20	chr10:43600862-43600912	HIPEpiC	eye:	n/a
21	chr10:43600239-43600289	AG09319	gingival:	n/a
22	chr10:43601916-43601966	AG10803	skin:	n/a
23	chr10:43596996-43597046	AG10803	skin:	n/a
24	chr10:43601862-43601912	HIPEpiC	eye:	n/a
25	chr10:43602387-43602437	SKMC	muscle:	n/a
26	chr10:43604667-43604717	PrEC	prostate:	n/a
27	chr10:43598772-43598822	AG04449	skin:	fetal
28	chr10:43603067-43603117	NHBE	bronchial:	n/a
29	chr10:43603918-43603968	H1-hESC	embryonic stem cell:	embryo
30	chr10:43600239-43600289	HEK293	kidney:	embryo
31	chr10:43599563-43599613	NH-A	brain:	n/a
32	chr10:43600239-43600289	A549	lung:	n/a
33	chr10:43603067-43603117	GM12878	blood:	n/a
34	chr10:43602387-43602437	AoSMC	blood vessel:	n/a
35	chr10:43596996-43597046	T-47D	breast:	n/a
36	chr10:43599566-43599616	HNPCEpiC	eye:	n/a
37	chr10:43601916-43601966	AG09309	skin:	n/a
38	chr10:43602387-43602437	ovcar-3	ovarian:	n/a
39	chr10:43603067-43603117	Hela-S3	cervix:	n/a
40	chr10:43600239-43600289	ovcar-3	ovarian:	n/a
41	chr10:43599476-43599526	BJ	skin:	n/a
42	chr10:43600239-43600289	IMR90	lung:	fetal
43	chr10:43600497-43600547	NHDF-neo	bronchial:	n/a
44	chr10:43603918-43603968	BJ	skin:	n/a
45	chr10:43599566-43599616	SK-N-MC	brain:	n/a
46	chr10:43601916-43601966	HNPCEpiC	eye:	n/a
47	chr10:43604667-43604717	NHDF-neo	bronchial:	n/a
48	chr10:43601862-43601912	Jurkat	blood:	n/a
49	chr10:43601862-43601912	Caco-2	colon:	n/a
50	chr10:43599476-43599526	Hepatocyte	liver:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:43361854..43362671-chr10:43600633..43601533,4	K562	blood:
2	chr10:43589023..43591875-chr10:43596909..43598786,2	MCF-7	breast:
3	chr10:43605967..43607514-chr10:43608103..43610558,2	MCF-7	breast:
4	chr10:43607653..43609397-chr10:43610018..43611648,2	MCF-7	breast:
5	chr10:43578198..43579973-chr10:43594655..43597408,2	MCF-7	breast:
6	chr10:43571287..43574219-chr10:43600622..43603596,3	MCF-7	breast:
7	chr10:43521500..43522685-chr10:43605254..43606963,53	MCF-7	breast:
8	chr10:43600575..43601274-chr8:145550248..145550759,2	NB4	blood:
9	chr10:43607653..43609397-chr10:43610018..43611648,2	MCF-7	breast:
10	chr10:43609230..43611797-chr10:43616396..43619297,2	K562	blood:
11	chr10:43607946..43610650-chr10:43632814..43635472,2	MCF-7	breast:
12	chr10:43601071..43602866-chr10:43603676..43605812,2	K562	blood:
13	chr10:43610105..43612462-chr19:13953320..13955874,2	MCF-7	breast:
14	chr10:43517462..43522124-chr10:43604454..43608281,5	MCF-7	breast:
15	chr10:43577015..43578995-chr10:43604341..43606597,2	MCF-7	breast:
16	chr10:43359833..43360692-chr10:43600708..43601545,3	MCF-7	breast:
17	chr10:43604452..43607562-chr10:43608780..43611078,3	K562	blood:
18	chr10:43602925..43605448-chr10:43606836..43609634,2	K562	blood:
19	chr10:43604834..43606698-chr10:43629827..43631473,2	MCF-7	breast:
20	chr10:43601071..43602866-chr10:43603676..43605812,2	K562	blood:
21	chr10:43368762..43369411-chr10:43606065..43606957,2	MCF-7	breast:
22	chr10:42673929..42674445-chr10:43600657..43601190,2	K562	blood:
23	chr10:43476503..43477844-chr10:43606043..43606921,3	MCF-7	breast:
24	chr10:43601833..43604723-chr10:43611468..43612976,2	MCF-7	breast:
25	chr10:43569624..43573381-chr10:43605727..43608957,3	MCF-7	breast:
26	chr10:43589765..43592695-chr10:43600961..43603100,2	MCF-7	breast:
27	chr10:43599513..43601509-chr10:43602516..43604753,2	MCF-7	breast:
28	chr10:43594982..43596781-chr10:43603444..43605896,2	MCF-7	breast:
29	chr10:43521557..43522557-chr10:43605823..43606953,34	MCF-7	breast:
30	chr10:43602925..43605448-chr10:43606836..43609634,2	K562	blood:
31	chr10:43594982..43596781-chr10:43603444..43605896,2	MCF-7	breast:
32	chr10:43571533..43575007-chr10:43595685..43599211,4	MCF-7	breast:
33	chr10:43574441..43574987-chr10:43601035..43601611,2	K562	blood:
34	chr10:43521524..43522456-chr10:43605890..43606964,14	MCF-7	breast:
35	chr10:43581616..43582507-chr10:43605989..43606921,3	MCF-7	breast:
36	chr10:43361928..43362761-chr10:43600658..43601529,2	MCF-7	breast:
37	chr10:43533165..43534049-chr10:43605965..43606922,5	MCF-7	breast:
38	chr10:43605967..43607514-chr10:43608103..43610558,2	MCF-7	breast:
39	chr10:43476552..43477542-chr10:43606341..43606847,2	MCF-7	breast:
40	chr10:43597660..43599265-chr10:43602367..43604242,2	K562	blood:
41	chr10:43600712..43601532-chr10:43751532..43752231,2	K562	blood:
42	chr10:43533165..43533679-chr10:43605965..43606922,3	MCF-7	breast:
43	chr10:43521915..43522534-chr10:43604245..43605068,2	MCF-7	breast:
44	chr10:43604452..43607562-chr10:43608780..43611078,3	K562	blood:
45	chr10:43602142..43604859-chr10:43903043..43904972,2	MCF-7	breast:
46	chr10:43587904..43589717-chr10:43600959..43603478,2	MCF-7	breast:
47	chr10:43597660..43599265-chr10:43602367..43604242,2	K562	blood:

No data

Variant related genes	Relation type
RET	TF binding region
RET	CpG island
ENSG00000229630	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000185000	chromatin interactions
ENSG00000273008	chromatin interactions
ENSG00000169826	chromatin interactions
ENSG00000169813	chromatin interactions

Extended variants
information (count: 708 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3026737	chr10:43596728-43596729	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536600216	chr10:43596789-43596790	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs145864887	chr10:43596823-43596824	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573390612	chr10:43596861-43596862	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs541264814	chr10:43596906-43596907	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs559258770	chr10:43596908-43596909	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577905706	chr10:43596915-43596916	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs370168725	chr10:43596943-43596944	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544993296	chr10:43596986-43596987	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs563548534	chr10:43596995-43596996	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73252043	chr10:43596997-43596998	Weak transcription Enhancers Bivalent Enhancer	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs2472738	chr10:43597088-43597089	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs561409155	chr10:43597102-43597103	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs528594481	chr10:43597125-43597126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs547200615	chr10:43597148-43597149	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184216084	chr10:43597156-43597157	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs548949321	chr10:43597174-43597175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532711384	chr10:43597202-43597203	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs190122671	chr10:43597213-43597214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569167372	chr10:43597226-43597227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182295359	chr10:43597303-43597304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111528123	chr10:43597318-43597319	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528659966	chr10:43597326-43597327	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs117421586	chr10:43597425-43597426	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373882660	chr10:43597440-43597441	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs34254989	chr10:43597459-43597460	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs398013307	chr10:43597465-43597466	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs201789764	chr10:43597466-43597467	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs534403032	chr10:43597479-43597480	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs553000295	chr10:43597506-43597507	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs112976896	chr10:43597589-43597590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs148863289	chr10:43597609-43597610	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs367850769	chr10:43597616-43597617	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs2742238	chr10:43597617-43597618	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs568108900	chr10:43597679-43597680	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs73252046	chr10:43597684-43597685	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs376004944	chr10:43597714-43597715	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs78838549	chr10:43597724-43597725	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185728832	chr10:43597758-43597759	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs375524825	chr10:43597780-43597781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76397662	chr10:43597793-43597794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs143083395	chr10:43597794-43597795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs267602487	chr10:43597803-43597804	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1800859	chr10:43597827-43597828	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs375576038	chr10:43597843-43597844	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs138265837	chr10:43597850-43597851	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs142345108	chr10:43597857-43597858	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs79014735	chr10:43597858-43597859	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551142665	chr10:43597883-43597884	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150261092	chr10:43597904-43597905	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43588400-43599400	Weak transcription	Pancreas	Pancrea
2	chr10:43589400-43596800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr10:43590600-43597600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr10:43591600-43599400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr10:43596400-43597600	Weak transcription	HUVEC	blood vessel
6	chr10:43596800-43597000	Bivalent Enhancer	Placenta	Placenta
7	chr10:43596800-43597000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
8	chr10:43596800-43598000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr10:43597000-43600200	Weak transcription	Right Atrium	heart
10	chr10:43597600-43597800	Enhancers	Spleen	Spleen
11	chr10:43597600-43598000	Enhancers	HUVEC	blood vessel
12	chr10:43597800-43598000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr10:43597800-43599800	Weak transcription	Spleen	Spleen
14	chr10:43598000-43598200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr10:43598200-43600000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:43598400-43598600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr10:43599400-43599600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr10:43599400-43600000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr10:43599400-43600000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr10:43599400-43600000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr10:43599400-43600000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr10:43599400-43600200	Bivalent Enhancer	Esophagus	oesophagus
23	chr10:43599400-43600400	Enhancers	Pancreas	Pancrea
24	chr10:43599800-43600000	Enhancers	Spleen	Spleen
25	chr10:43599800-43600200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
26	chr10:43600000-43600200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr10:43600000-43600200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr10:43600000-43600200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr10:43600000-43600200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
30	chr10:43600000-43600200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
31	chr10:43600000-43600200	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr10:43600000-43600200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr10:43600000-43600200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
34	chr10:43600000-43600200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
35	chr10:43600000-43600200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr10:43600000-43600200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
37	chr10:43600000-43600200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr10:43600000-43600200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
39	chr10:43600000-43600200	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
40	chr10:43600000-43600200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
41	chr10:43600000-43600200	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr10:43600000-43600200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
43	chr10:43600000-43600200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr10:43600000-43600200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr10:43600000-43600200	Bivalent Enhancer	Adipose Nuclei	Adipose
46	chr10:43600000-43600200	Enhancers	Brain Angular Gyrus	brain
47	chr10:43600000-43600200	Bivalent Enhancer	Brain Anterior Caudate	brain
48	chr10:43600000-43600200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
49	chr10:43600000-43600200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr10:43600000-43600200	Bivalent Enhancer	Colonic Mucosa	Colon

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