Variant report

Variant	nsv549894
Chromosome Location	chr10:5708801-5721653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:272)
CpG islands
(count:305)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5710369-5710645	HepG2	liver:	n/a	n/a
2	ATF3	chr10:5708602-5709006	A549	lung:	n/a	n/a
3	ATF3	chr10:5708448-5708805	K562	blood:	n/a	n/a
4	BCL3	chr10:5708858-5709224	GM12878	blood:	n/a	n/a
5	BCL3	chr10:5708804-5709189	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:5708587-5709192	K562	blood:	n/a	n/a
7	BHLHE40	chr10:5711632-5711940	K562	blood:	n/a	n/a
8	BHLHE40	chr10:5708641-5709243	HepG2	liver:	n/a	n/a
9	BRCA1	chr10:5708655-5708931	HepG2	liver:	n/a	n/a
10	BRCA1	chr10:5708541-5708817	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr10:5716240-5716561	K562	blood:	n/a	n/a
12	CCNT2	chr10:5707836-5708803	K562	blood:	n/a	n/a
13	CCNT2	chr10:5711612-5711848	K562	blood:	n/a	n/a
14	CEBPB	chr10:5707396-5708828	Hela-S3	cervix:	n/a	chr10:5707632-5707643
15	CEBPB	chr10:5712748-5712793	A549	lung:	n/a	n/a
16	CEBPB	chr10:5717598-5717785	K562	blood:	n/a	n/a
17	CHD2	chr10:5720631-5720702	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr10:5708383-5708857	K562	blood:	n/a	n/a
19	CHD2	chr10:5708490-5708868	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr10:5708549-5709109	HepG2	liver:	n/a	n/a
21	CREB1	chr10:5708369-5709199	HepG2	liver:	n/a	n/a
22	CREB1	chr10:5708000-5709299	HepG2	liver:	n/a	n/a
23	CREB1	chr10:5708383-5709009	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr10:5708362-5708987	K562	blood:	n/a	n/a
25	CREB1	chr10:5708368-5708964	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr10:5708378-5708883	GM12878	blood:	n/a	n/a
27	CREB1	chr10:5707941-5708998	K562	blood:	n/a	n/a
28	CREB1	chr10:5708340-5708823	A549	lung:	n/a	n/a
29	CTCF	chr10:5721640-5721790	SAEC	small airway:	n/a	n/a
30	CTCF	chr10:5721640-5721790	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr10:5708616-5708805	A549	lung:	n/a	n/a
32	CTCF	chr10:5721580-5721730	RPTEC	kidney:	n/a	n/a
33	CTCF	chr10:5721573-5721910	IMR90	lung:	n/a	n/a
34	CTCF	chr10:5708775-5708830	ProgFib	skin:	n/a	n/a
35	CTCF	chr10:5721600-5721750	Caco-2	colon:	n/a	n/a
36	CTCF	chr10:5721640-5721790	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr10:5721580-5721730	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr10:5708653-5708823	MCF-7	breast:	n/a	n/a
39	CTCF	chr10:5708840-5708990	BJ	skin:	n/a	n/a
40	CTCF	chr10:5708593-5708872	GM19239	blood:	n/a	n/a
41	CTCF	chr10:5708660-5708810	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr10:5721640-5721790	HMF	breast:	n/a	n/a
43	CTCF	chr10:5721640-5721790	HepG2	liver:	n/a	n/a
44	CTCF	chr10:5708660-5708810	HMEC	breast:	n/a	n/a
45	CTCF	chr10:5708720-5708870	HRE	kidney:	n/a	n/a
46	CTCF	chr10:5721618-5721808	HepG2	liver:	n/a	n/a
47	CTCF	chr10:5721600-5721750	HPF	lung:	n/a	n/a
48	CTCF	chr10:5708513-5708870	K562	blood:	n/a	n/a
49	CTCF	chr10:5708760-5708910	A549	lung:	n/a	n/a
50	CTCF	chr10:5721620-5721770	HCFaa	heart:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5708797-5708847	Hela-S3	cervix:	n/a
2	chr10:5708825-5708875	GM12892	blood:	n/a
3	chr10:5708825-5708875	HAEpiC	amniotic membrane:	n/a
4	chr10:5708765-5708815	U87	brain:	n/a
5	chr10:5708881-5708931	HCF	heart:	n/a
6	chr10:5708825-5708875	MCF10A-Er-Src	breast:	n/a
7	chr10:5708797-5708847	SKMC	muscle:	n/a
8	chr10:5710888-5710938	ovcar-3	ovarian:	n/a
9	chr10:5708797-5708847	HepG2	liver:	n/a
10	chr10:5708881-5708931	HNPCEpiC	eye:	n/a
11	chr10:5708825-5708875	PANC-1	pancreas:	n/a
12	chr10:5708797-5708847	AoSMC	blood vessel:	n/a
13	chr10:5708881-5708931	AG04450	lung:	fetal
14	chr10:5708825-5708875	A549	lung:	n/a
15	chr10:5710888-5710938	NHDF-neo	bronchial:	n/a
16	chr10:5708881-5708931	BJ	skin:	n/a
17	chr10:5708881-5708931	IMR90	lung:	fetal
18	chr10:5708881-5708931	Hela-S3	cervix:	n/a
19	chr10:5708825-5708875	GM06990	blood:	n/a
20	chr10:5708825-5708875	PrEC	prostate:	n/a
21	chr10:5708765-5708815	ECC-1	luminal epithelium:	n/a
22	chr10:5708881-5708931	GM19239	blood:	n/a
23	chr10:5708797-5708847	HCM	heart:	n/a
24	chr10:5708765-5708815	SKMC	muscle:	n/a
25	chr10:5708797-5708847	GM06990	blood:	n/a
26	chr10:5708765-5708815	NHBE	bronchial:	n/a
27	chr10:5710888-5710938	ECC-1	luminal epithelium:	n/a
28	chr10:5708825-5708875	BE2_C	brain:	n/a
29	chr10:5708881-5708931	MCF-7	breast:	n/a
30	chr10:5708765-5708815	Jurkat	blood:	n/a
31	chr10:5708881-5708931	HCPEpiC	choroid plexus:	n/a
32	chr10:5708825-5708875	Jurkat	blood:	n/a
33	chr10:5708797-5708847	T-47D	breast:	n/a
34	chr10:5710888-5710938	SK-N-SH	brain:	n/a
35	chr10:5710888-5710938	HIPEpiC	eye:	n/a
36	chr10:5708881-5708931	Jurkat	blood:	n/a
37	chr10:5708825-5708875	HCF	heart:	n/a
38	chr10:5708825-5708875	HMEC	breast:	n/a
39	chr10:5708797-5708847	ECC-1	luminal epithelium:	n/a
40	chr10:5710888-5710938	HRE	kidney:	n/a
41	chr10:5708825-5708875	SK-N-SH_RA	brain:	n/a
42	chr10:5708797-5708847	AG09319	gingival:	n/a
43	chr10:5710888-5710938	HCT-116	colon:	n/a
44	chr10:5710888-5710938	SK-N-SH_RA	brain:	n/a
45	chr10:5708881-5708931	Hepatocyte	liver:	n/a
46	chr10:5708797-5708847	HRPEpiC	eye:	n/a
47	chr10:5708765-5708815	HCF	heart:	n/a
48	chr10:5708825-5708875	ProgFib	skin:	n/a
49	chr10:5708825-5708875	HepG2	liver:	n/a
50	chr10:5708825-5708875	CMK	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5534278..5536175-chr10:5709413..5711333,2	MCF-7	breast:
2	chr10:5707719..5709670-chr10:5755550..5758097,2	MCF-7	breast:
3	chr10:5702205..5703969-chr10:5719361..5720928,2	K562	blood:
4	chr10:5708070..5709600-chr10:5714196..5716454,2	K562	blood:
5	chr10:5719967..5722164-chr10:5733204..5735330,2	K562	blood:
6	chr10:5708283..5708927-chr16:31470241..31471151,2	Hela-S3	cervix:
7	chr10:5691219..5693694-chr10:5706407..5709884,5	K562	blood:
8	chr10:5708441..5709982-chr10:5853880..5856185,2	K562	blood:
9	chr10:5706412..5710020-chr10:5717642..5721697,4	K562	blood:
10	chr1:45186983..45187584-chr10:5717282..5717804,2	Hela-S3	cervix:
11	chr10:5707112..5709350-chr10:5721033..5724526,3	MCF-7	breast:
12	chr10:5708145..5711332-chr10:5711422..5714453,3	K562	blood:
13	chr10:5714237..5717249-chr10:5724981..5728429,5	MCF-7	breast:
14	chr10:5706894..5712025-chr10:5724987..5728504,7	MCF-7	breast:
15	chr10:5659171..5662010-chr10:5707160..5709672,2	MCF-7	breast:
16	chr10:5539704..5542101-chr10:5707355..5709721,2	MCF-7	breast:
17	chr10:5707879..5710257-chr22:29195153..29198012,2	MCF-7	breast:
18	chr10:5711853..5714027-chr10:5850909..5854727,3	K562	blood:
19	chr10:5682936..5684955-chr10:5707223..5709652,2	MCF-7	breast:
20	chr10:5707177..5709381-chr10:5931479..5933432,3	MCF-7	breast:
21	chr10:5691710..5696017-chr10:5704918..5709884,5	K562	blood:
22	chr10:5711268..5714710-chr10:5724793..5726863,3	K562	blood:
23	chr10:5593662..5596441-chr10:5715811..5718225,2	MCF-7	breast:
24	chr10:5719546..5721804-chr10:5852242..5853949,2	K562	blood:
25	chr10:5713284..5716220-chr10:5720012..5722178,2	MCF-7	breast:
26	chr10:5693035..5694610-chr10:5707136..5708829,2	MCF-7	breast:
27	chr10:5707157..5710880-chr10:5853405..5856185,3	K562	blood:
28	chr10:5705929..5709970-chr10:5717272..5720896,4	MCF-7	breast:
29	chr10:5708731..5711725-chr10:5733293..5735227,2	MCF-7	breast:
30	chr10:5694643..5697426-chr10:5716773..5718834,2	K562	blood:
31	chr10:5704732..5708288-chr10:5710770..5713628,5	K562	blood:
32	chr10:5713284..5716220-chr10:5720012..5722178,2	MCF-7	breast:
33	chr10:5707419..5708953-chr10:5931052..5933501,2	MCF-7	breast:
34	chr10:5715613..5722636-chr10:5722933..5730555,14	MCF-7	breast:
35	chr10:5486439..5489849-chr10:5706503..5709188,4	MCF-7	breast:
36	chr10:5707969..5709619-chr10:5713613..5715231,2	MCF-7	breast:
37	chr10:5710108..5711995-chr10:5854432..5856074,2	MCF-7	breast:
38	chr10:5704788..5710194-chr10:5724908..5728833,8	K562	blood:
39	chr10:5706900..5709374-chr10:5740250..5741979,2	MCF-7	breast:
40	chr10:5487870..5492604-chr10:5704699..5710397,11	MCF-7	breast:

No data

Variant related genes	Relation type
ASB13	TF binding region
ASB13	CpG island
ENSG00000108021	chromatin interactions
ENSG00000196372	chromatin interactions
ENSG00000260267	chromatin interactions
ENSG00000228951	chromatin interactions
ENSG00000134461	chromatin interactions
ENSG00000178372	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000134452	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000100219	chromatin interactions
ENSG00000226647	chromatin interactions
ENSG00000140691	chromatin interactions
ENSG00000272764	chromatin interactions

Extended variants
information (count: 486 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3814204	chr10:5708801-5708802	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531918743	chr10:5708809-5708810	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
3	rs150465157	chr10:5708824-5708825	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
4	rs137976302	chr10:5708853-5708854	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
5	rs3814203	chr10:5708896-5708897	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs112101468	chr10:5709012-5709013	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs3814202	chr10:5709026-5709027	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs559561469	chr10:5709036-5709037	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs199973385	chr10:5709037-5709038	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs536757043	chr10:5709067-5709068	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs142501752	chr10:5709132-5709133	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs376641106	chr10:5709149-5709150	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs3814200	chr10:5709151-5709152	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs532815331	chr10:5709165-5709166	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
15	rs551683402	chr10:5709226-5709227	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs5019339	chr10:5709288-5709289	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs181872165	chr10:5709290-5709291	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
18	rs75555247	chr10:5709306-5709307	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
19	rs186546995	chr10:5709327-5709328	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
20	rs559739686	chr10:5709333-5709334	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
21	rs201028713	chr10:5709385-5709386	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs5019340	chr10:5709387-5709388	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs545735710	chr10:5709402-5709403	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs192331162	chr10:5709423-5709424	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs542348852	chr10:5709430-5709431	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs183702943	chr10:5709441-5709442	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs567368152	chr10:5709513-5709514	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs185161054	chr10:5709533-5709534	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs550343198	chr10:5709631-5709632	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs2386639	chr10:5709659-5709660	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs565298240	chr10:5709678-5709679	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs532845240	chr10:5709680-5709681	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs552848771	chr10:5709690-5709691	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs189623307	chr10:5709715-5709716	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs73610532	chr10:5709740-5709741	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs79390427	chr10:5709752-5709753	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs548743588	chr10:5709768-5709769	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs570126585	chr10:5709802-5709803	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs3814199	chr10:5709846-5709847	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs2386638	chr10:5709847-5709848	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs2386637	chr10:5709909-5709910	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs386740381	chr10:5709957-5709958	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs2892075	chr10:5709959-5709960	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs571737461	chr10:5709979-5709980	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs74939461	chr10:5709981-5709982	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs138531389	chr10:5709994-5709995	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs543106471	chr10:5710006-5710007	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs565498629	chr10:5710042-5710043	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs374273246	chr10:5710043-5710044	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs532580794	chr10:5710044-5710045	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5707400-5709000	Active TSS	Psoas Muscle	Psoas
2	chr10:5707400-5709200	Active TSS	Fetal Stomach	stomach
3	chr10:5707400-5709400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr10:5707600-5709000	Active TSS	Right Atrium	heart
5	chr10:5707600-5709200	Active TSS	HSMMtube	muscle
6	chr10:5707800-5709000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr10:5707800-5709000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr10:5707800-5709000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr10:5707800-5709000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
10	chr10:5707800-5709000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr10:5707800-5709200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:5708000-5709000	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr10:5708200-5709000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr10:5708200-5709000	Active TSS	Thymus	Thymus
15	chr10:5708600-5709000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:5708600-5709000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr10:5708600-5709000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr10:5708600-5709000	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
19	chr10:5708600-5709000	Flanking Active TSS	Esophagus	oesophagus
20	chr10:5708600-5709000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
21	chr10:5708600-5709000	Flanking Active TSS	Fetal Muscle Trunk	muscle
22	chr10:5708600-5709000	Flanking Active TSS	Placenta	Placenta
23	chr10:5708600-5709000	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
24	chr10:5708600-5709000	Flanking Active TSS	Placenta Amnion	Placenta Amnion
25	chr10:5708600-5709000	Flanking Active TSS	Right Ventricle	heart
26	chr10:5708600-5709000	Flanking Active TSS	Stomach Mucosa	stomach
27	chr10:5708600-5709000	Flanking Active TSS	Osteobl	bone
28	chr10:5708600-5709200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr10:5708600-5709200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
30	chr10:5708600-5709200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
31	chr10:5708600-5709200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
32	chr10:5708600-5709200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
33	chr10:5708600-5709200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr10:5708600-5709200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr10:5708600-5709200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr10:5708600-5709200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr10:5708600-5709200	Flanking Active TSS	Adipose Nuclei	Adipose
38	chr10:5708600-5709200	Flanking Active TSS	Liver	Liver
39	chr10:5708600-5709200	Flanking Active TSS	Gastric	stomach
40	chr10:5708600-5709200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
41	chr10:5708600-5709200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr10:5708600-5709200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr10:5708600-5709200	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
44	chr10:5708600-5709200	Flanking Active TSS	HMEC	breast
45	chr10:5708600-5709200	Flanking Active TSS	NH-A	brain
46	chr10:5708600-5709400	Flanking Bivalent TSS/Enh	Dnd41	blood
47	chr10:5708600-5709600	Flanking Active TSS	HepG2	liver
48	chr10:5708600-5709600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr10:5708600-5709800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr10:5708800-5709000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell

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