Variant report

Variant	rs703017
Chromosome Location	chr10:28619922-28619923
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10826432	0.82[CHB][hapmap]
rs11006935	1.00[CHB][hapmap]
rs11006941	1.00[CHB][hapmap]
rs11006942	1.00[CHB][hapmap]
rs11006948	1.00[CHB][hapmap]
rs11006971	1.00[CHB][hapmap]
rs1148182	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs1148183	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs1148185	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs1148186	0.82[JPT][hapmap]
rs1148189	0.88[AFR][1000 genomes]
rs12254745	1.00[CHB][hapmap]
rs12358648	1.00[CHB][hapmap]
rs1418758	0.82[CHB][hapmap]
rs16928633	1.00[CHB][hapmap]
rs2100614	0.82[CHB][hapmap]
rs703015	0.89[ASN][1000 genomes]
rs703016	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7070175	1.00[CHB][hapmap]
rs7073107	0.82[CHB][hapmap]
rs7078271	1.00[CHB][hapmap]
rs7100335	1.00[CHB][hapmap]
rs786392	0.89[ASN][1000 genomes]
rs786397	0.89[ASN][1000 genomes]
rs786399	0.89[ASN][1000 genomes]
rs7898888	0.85[JPT][hapmap]
rs7911615	1.00[CHB][hapmap]
rs7916525	1.00[CHB][hapmap]
rs811496	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1041555	chr10:28419399-29304934	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv1037863	chr10:28419399-29378871	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv540521	chr10:28419399-29378871	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1044938	chr10:28601993-28659440	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28614800-28620600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
2	chr10:28615000-28620000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr10:28615200-28621000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr10:28616000-28621600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:28616400-28620800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr10:28616800-28620600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr10:28616800-28623000	Weak transcription	Fetal Muscle Leg	muscle
8	chr10:28616800-28623800	Weak transcription	NHLF	lung
9	chr10:28617000-28620600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr10:28617000-28621000	Enhancers	Colon Smooth Muscle	Colon
11	chr10:28617000-28621600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:28617000-28621600	Weak transcription	Pancreas	Pancrea
13	chr10:28617000-28622800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr10:28617200-28621000	Weak transcription	NH-A	brain
15	chr10:28617400-28621000	Weak transcription	HMEC	breast
16	chr10:28617600-28621000	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr10:28617600-28621000	Weak transcription	HSMM	muscle
18	chr10:28617800-28621000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:28617800-28622600	Weak transcription	NHEK	skin
20	chr10:28617800-28623000	Weak transcription	Fetal Stomach	stomach
21	chr10:28618000-28620200	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr10:28618200-28620600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr10:28618200-28621000	Weak transcription	HSMMtube	muscle
24	chr10:28618200-28621200	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr10:28618600-28620800	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr10:28618600-28621600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr10:28618600-28621800	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr10:28618800-28620600	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr10:28618800-28621000	Enhancers	Primary T cells fromperipheralblood	blood
30	chr10:28618800-28621000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr10:28618800-28621000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr10:28618800-28621800	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr10:28618800-28624400	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr10:28618800-28626600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr10:28619000-28620000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr10:28619000-28621200	Enhancers	Primary B cells from cord blood	blood
37	chr10:28619000-28621800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr10:28619000-28624600	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr10:28619200-28624600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr10:28619400-28621200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr10:28619400-28624600	Enhancers	Primary hematopoietic stem cells	blood
42	chr10:28619600-28621800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr10:28619800-28620000	Enhancers	Primary T cells from cord blood	blood
44	chr10:28619800-28620200	Enhancers	Rectal Smooth Muscle	rectum
45	chr10:28619800-28620400	Enhancers	Primary B cells from peripheral blood	blood
46	chr10:28619800-28621600	Weak transcription	Fetal Thymus	thymus

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