Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10784252	0.92[CEU][hapmap]
rs10784263	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10784264	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1395489	0.92[CEU][hapmap]
rs1869893	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2168452	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2198779	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2360681	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6581418	0.92[CEU][hapmap]
rs6581426	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6581430	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs6581431	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6581432	1.00[CEU][hapmap]
rs7398155	0.92[CEU][hapmap]
rs7487386	1.00[CEU][hapmap]
rs7957259	1.00[CEU][hapmap]
rs7960162	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7974958	0.85[CEU][hapmap]
rs7977950	1.00[CEU][hapmap]
rs973121	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][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	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No data

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