Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1018991	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.84[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap]
rs10236330	0.83[CHB][hapmap];0.82[CHD][hapmap]
rs10236878	0.82[YRI][hapmap]
rs10282302	0.80[MKK][hapmap]
rs12113038	0.82[LWK][hapmap];0.81[MKK][hapmap]
rs13230403	0.94[CHD][hapmap]
rs1585815	0.89[GIH][hapmap];0.84[MEX][hapmap];0.81[TSI][hapmap]
rs6464815	1.00[CEU][hapmap];0.94[CHD][hapmap];0.93[GIH][hapmap];0.91[TSI][hapmap];0.84[EUR][1000 genomes]
rs6973129	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6973308	0.82[LWK][hapmap];0.81[MKK][hapmap]
rs700296	0.82[GIH][hapmap]
rs700299	0.86[GIH][hapmap];0.84[MEX][hapmap];0.81[TSI][hapmap]
rs700308	0.82[GIH][hapmap];0.81[TSI][hapmap]
rs7778880	1.00[CEU][hapmap];0.83[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap]
rs7779464	1.00[CEU][hapmap];0.83[CHB][hapmap];0.81[JPT][hapmap]
rs7780096	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap]
rs7796301	0.83[CHB][hapmap];0.85[CHD][hapmap];0.83[JPT][hapmap]
rs826651	0.84[MEX][hapmap];0.81[TSI][hapmap]
rs826655	0.86[GIH][hapmap];0.84[MEX][hapmap];0.81[TSI][hapmap]
rs826657	0.86[GIH][hapmap];0.84[MEX][hapmap];0.81[TSI][hapmap]
rs826660	0.89[GIH][hapmap];0.84[MEX][hapmap];0.81[TSI][hapmap]
rs826786	0.82[GIH][hapmap]

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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10267232	OR6B1	cis	parietal	SCAN

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

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