Variant report

Variant	rs1021932
Chromosome Location	chr3:94765429-94765430
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1017370	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10212430	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10804440	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1120672	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11706789	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11707669	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11710300	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11718955	0.91[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11719000	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11720623	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11918258	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11919926	0.92[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes]
rs1368193	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1432468	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1432473	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1529652	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1529654	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1549860	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1835872	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1897461	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1991752	0.87[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes]
rs1991753	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs2116611	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2370168	0.80[EUR][1000 genomes]
rs300090	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs300301	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs300306	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs380053	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs4857128	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4857129	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs49698	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6437515	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs728066	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7624843	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7625912	0.84[EUR][1000 genomes]
rs7626615	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7626749	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7627012	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs7627313	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7631515	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7634882	0.88[EUR][1000 genomes]
rs7635097	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9714169	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9809325	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9813195	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9822197	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9822600	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9827377	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9830733	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9830753	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9830901	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9838383	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9850418	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9854077	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9857434	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs9861234	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9861368	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9880324	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs991552	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877169	chr3:94675697-94840854	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv590993	chr3:94759504-94841342	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:94760600-94767000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links