Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10500627	0.84[EUR][1000 genomes]
rs10768352	1.00[YRI][hapmap]
rs10836934	0.85[EUR][1000 genomes]
rs10836949	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10836950	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10836954	1.00[CEU][hapmap];0.91[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10836955	0.91[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[ASN][1000 genomes]
rs10836956	1.00[CEU][hapmap];0.91[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[ASN][1000 genomes]
rs11034193	1.00[YRI][hapmap]
rs11034428	1.00[YRI][hapmap]
rs11034435	1.00[CEU][hapmap]
rs11034563	1.00[YRI][hapmap]
rs11034596	0.85[EUR][1000 genomes]
rs11034602	0.85[EUR][1000 genomes]
rs11034615	1.00[YRI][hapmap]
rs11034658	0.92[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11034672	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[ASN][1000 genomes]
rs11601065	1.00[YRI][hapmap]
rs12273277	1.00[YRI][hapmap]
rs12276692	1.00[YRI][hapmap]
rs12291286	1.00[YRI][hapmap]
rs12364864	1.00[YRI][hapmap]
rs4910693	1.00[YRI][hapmap]
rs9633907	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][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	nsv1054847	chr11:4642875-5200656	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
2	esv2758254	chr11:4907893-5135331	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
3	esv2759799	chr11:4907893-5135331	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases

No data

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

No data

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