Variant report

Variant	rs7910594
Chromosome Location	chr10:90188027-90188028
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs1067839	0.92[CEU][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1067840	0.92[CEU][hapmap];0.91[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10736351	0.92[CEU][hapmap];0.81[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10736352	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10736354	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10749589	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10749590	0.92[CEU][hapmap];0.96[CHB][hapmap];0.87[JPT][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10749591	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10788598	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10788599	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10788600	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10788602	0.92[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10887817	0.81[CEU][hapmap];0.88[EUR][1000 genomes]
rs10887818	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs10887821	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10887823	0.92[CEU][hapmap];0.96[CHB][hapmap];0.87[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10887824	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1169043	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1342450	0.92[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1342451	0.82[CEU][hapmap]
rs1342456	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1578696	0.96[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1617881	0.82[CEU][hapmap]
rs1750274	0.88[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1935579	0.92[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1935581	0.96[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1935582	0.96[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1935584	0.99[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2096194	0.91[CEU][hapmap];0.95[CHB][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2185786	0.88[CEU][hapmap];0.81[JPT][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2312610	0.92[CEU][hapmap];0.96[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2433340	0.92[CEU][hapmap];0.87[EUR][1000 genomes]
rs2437875	0.82[JPT][hapmap];0.90[AMR][1000 genomes]
rs2477954	0.90[AMR][1000 genomes]
rs2477956	0.89[CEU][hapmap];0.83[JPT][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2576169	0.90[AMR][1000 genomes]
rs2576170	0.83[JPT][hapmap];0.90[AMR][1000 genomes]
rs2576171	0.82[JPT][hapmap];0.90[AMR][1000 genomes]
rs2576172	0.81[JPT][hapmap];0.90[AMR][1000 genomes]
rs2576176	0.82[JPT][hapmap]
rs2576181	0.88[CEU][hapmap];0.85[JPT][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2872092	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4509673	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4596981	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4606392	1.00[CEU][hapmap];0.96[CHB][hapmap];0.87[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4619060	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4933480	0.82[EUR][1000 genomes]
rs4934403	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs4934404	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4934409	0.92[CEU][hapmap];0.96[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4934411	0.92[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6586132	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs6586134	0.82[CEU][hapmap]
rs6586139	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7899828	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7907732	0.90[EUR][1000 genomes]
rs7909697	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7911996	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7918921	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs7921352	0.88[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs792205	0.82[CEU][hapmap]
rs792207	0.81[CEU][hapmap];0.83[EUR][1000 genomes]
rs792208	0.92[CEU][hapmap];0.82[JPT][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs792209	0.81[CEU][hapmap]
rs792211	0.99[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs792213	0.82[CEU][hapmap];0.83[EUR][1000 genomes]
rs792214	0.89[CEU][hapmap];0.99[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs792215	1.00[CEU][hapmap];0.81[YRI][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs792230	0.82[CEU][hapmap]
rs792234	0.85[CEU][hapmap]
rs792235	0.92[CEU][hapmap];0.82[YRI][hapmap];0.99[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7922551	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs796945	0.80[CEU][hapmap]
rs806694	0.92[CEU][hapmap];0.99[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs813782	0.92[CEU][hapmap];0.99[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs814242	0.99[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895879	chr10:90015725-90219298	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv482385	chr10:90066140-90259751	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv948664	chr10:90076715-90517150	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1054984	chr10:90122512-90278038	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1050587	chr10:90146582-90272627	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv540739	chr10:90146582-90272627	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90186400-90189400	Enhancers	Hela-S3	cervix
2	chr10:90186600-90188400	Weak transcription	Psoas Muscle	Psoas
3	chr10:90186800-90188600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr10:90187400-90188200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr10:90187600-90188200	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr10:90187600-90188800	Enhancers	Adipose Nuclei	Adipose
7	chr10:90187600-90189400	Enhancers	A549	lung
8	chr10:90187800-90188800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr10:90188000-90188200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:90188000-90188200	Enhancers	HSMMtube	muscle
11	chr10:90188000-90188400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:90188000-90188800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr10:90188000-90188800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr10:90188000-90188800	Enhancers	NHDF-Ad	bronchial
15	chr10:90188000-90188800	Enhancers	Osteobl	bone
16	chr10:90188000-90189000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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