Variant report

Variant	rs3816536
Chromosome Location	chr2:173543380-173543381
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10166107	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10166642	0.80[EUR][1000 genomes]
rs10172894	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10178654	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10180021	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10188207	1.00[ASN][1000 genomes]
rs10188540	0.85[ASN][1000 genomes]
rs10190099	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10198425	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10198426	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10198546	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10199472	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10201129	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10202550	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10205076	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10205126	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10208151	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10209860	0.95[ASN][1000 genomes]
rs10210195	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10210546	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11887454	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11887904	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11888564	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11890159	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11891071	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11894913	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11895461	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11897396	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11898565	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11899594	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11902043	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11904366	1.00[JPT][hapmap]
rs12328591	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12328781	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12329241	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12693005	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13007707	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13384609	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13385403	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13385676	0.85[ASN][1000 genomes]
rs13387816	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13389072	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13392808	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13394924	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13400719	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13408965	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13411408	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13415156	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13417334	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13417913	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13420845	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13422388	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13423248	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13425350	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13427701	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13427921	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13428122	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13432176	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1451447	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1597647	0.81[EUR][1000 genomes]
rs16860696	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16860697	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17299956	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17702263	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1839767	0.80[EUR][1000 genomes]
rs1869922	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2167374	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28541707	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28670307	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28690076	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56308044	0.80[EUR][1000 genomes]
rs57104776	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59648896	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62168072	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62169318	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62169319	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62169322	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62169323	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62169324	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62169325	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62169326	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6712686	0.95[ASN][1000 genomes]
rs6717366	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6717851	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6723872	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6724116	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6741433	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6752257	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6757567	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7573946	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	esv2760591	chr2:173396905-173719520	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv583665	chr2:173460640-173643087	Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173539600-173554200	Weak transcription	Primary T cells from cord blood	blood
2	chr2:173541800-173543600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr2:173543000-173545400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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