Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10259368	0.88[CEU][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1525218	0.82[CEU][hapmap]
rs1525219	0.84[CEU][hapmap]
rs1528507	0.86[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1528519	0.87[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1528521	0.86[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1528523	0.82[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1528524	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1585816	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs1608786	0.84[CEU][hapmap]
rs1819068	1.00[CEU][hapmap];0.83[CHB][hapmap];0.81[JPT][hapmap]
rs1950033	0.84[CEU][hapmap]
rs2286125	0.86[CEU][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2888505	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs4467862	0.84[CEU][hapmap]
rs4725717	0.84[CEU][hapmap]
rs4725736	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4726854	0.84[CEU][hapmap]
rs4726858	0.84[CEU][hapmap]
rs4726875	0.86[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6464796	0.84[CEU][hapmap]
rs6948780	0.84[CEU][hapmap]
rs7782445	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7795712	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7796028	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7800366	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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