Variant report

Variant	rs3906013
Chromosome Location	chr3:179981971-179981972
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10222466	0.93[EUR][1000 genomes]
rs10513771	0.90[ASN][1000 genomes]
rs10937020	0.84[EUR][1000 genomes]
rs10937021	0.90[EUR][1000 genomes]
rs11709960	0.85[EUR][1000 genomes]
rs12486206	0.83[ASN][1000 genomes]
rs12487650	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12491089	0.84[ASN][1000 genomes]
rs12497420	0.89[ASN][1000 genomes]
rs12636328	0.88[EUR][1000 genomes]
rs12638851	0.83[ASN][1000 genomes]
rs12638877	0.84[ASN][1000 genomes]
rs13322790	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1357904	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1404744	0.82[EUR][1000 genomes]
rs1464844	0.98[EUR][1000 genomes]
rs1464845	0.90[ASN][1000 genomes]
rs1525269	0.97[EUR][1000 genomes]
rs1525272	0.99[EUR][1000 genomes]
rs1525276	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1525277	0.84[EUR][1000 genomes]
rs1568859	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1581549	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1589858	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16831288	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16831406	0.81[ASN][1000 genomes]
rs1852121	0.83[EUR][1000 genomes]
rs1852122	0.83[EUR][1000 genomes]
rs1852123	0.99[EUR][1000 genomes]
rs2091273	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2337368	0.80[ASN][1000 genomes]
rs2339967	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2339968	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2878954	0.88[ASN][1000 genomes]
rs28865282	0.85[EUR][1000 genomes]
rs3849420	0.88[EUR][1000 genomes]
rs3906014	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3914867	0.87[ASN][1000 genomes]
rs3914868	0.87[ASN][1000 genomes]
rs4109306	0.99[EUR][1000 genomes]
rs4241377	0.93[ASN][1000 genomes]
rs4854902	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4854903	0.90[ASN][1000 genomes]
rs4854907	0.82[AFR][1000 genomes]
rs4854961	0.85[EUR][1000 genomes]
rs4854962	0.85[EUR][1000 genomes]
rs4854964	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4854966	0.90[ASN][1000 genomes]
rs56234136	0.90[ASN][1000 genomes]
rs62292283	0.89[ASN][1000 genomes]
rs62292284	0.89[ASN][1000 genomes]
rs62292290	0.90[ASN][1000 genomes]
rs62292291	0.90[ASN][1000 genomes]
rs62292292	0.93[ASN][1000 genomes]
rs62292326	0.83[ASN][1000 genomes]
rs6790229	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6790465	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs7619775	0.97[EUR][1000 genomes]
rs7621628	0.87[EUR][1000 genomes]
rs7622125	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7622865	0.80[ASN][1000 genomes]
rs7639931	0.93[ASN][1000 genomes]
rs7643438	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7644566	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs7652322	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7652473	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9290696	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9290697	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs939440	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs939441	0.82[CEU][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap]
rs939442	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs9683358	0.83[ASN][1000 genomes]
rs9812621	0.96[EUR][1000 genomes]
rs9819178	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9821124	0.85[EUR][1000 genomes]
rs9837718	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9840477	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9840775	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9845934	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs9860526	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9862989	0.80[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs9864555	0.86[EUR][1000 genomes]
rs9868908	0.84[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs9869517	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9869873	0.93[ASN][1000 genomes]
rs9871936	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9877454	0.98[EUR][1000 genomes]
rs9880357	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012271	chr3:179806875-180234871	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv878040	chr3:179823887-180128288	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv997388	chr3:179899279-180172349	Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv536817	chr3:179899279-180172349	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179979400-179985200	Weak transcription	HMEC	breast
2	chr3:179980600-179992400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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