Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10251488	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs10276658	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs11505677	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs11764538	1.00[CHB][hapmap]
rs11772135	1.00[CHB][hapmap]
rs12703911	1.00[CHB][hapmap]
rs12703916	1.00[CHB][hapmap]
rs12703921	1.00[CHB][hapmap]
rs12703922	1.00[CHB][hapmap]
rs13221977	1.00[CHB][hapmap]
rs13235407	1.00[CHB][hapmap]
rs13235593	1.00[CHB][hapmap]
rs17170636	1.00[CHB][hapmap]
rs17223460	1.00[CHB][hapmap]
rs17224658	1.00[CHB][hapmap]
rs1860135	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs1860136	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1990251	1.00[CHB][hapmap]
rs2046052	1.00[CHB][hapmap]
rs2373128	1.00[CHB][hapmap]
rs2373129	1.00[CHB][hapmap]
rs28432729	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4272288	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6947112	1.00[CHB][hapmap]
rs6955567	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7788405	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs995309	0.89[AFR][1000 genomes];1.00[ASN][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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