Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11174243	1.00[EUR][1000 genomes]
rs11174248	1.00[EUR][1000 genomes]
rs11174249	0.92[YRI][hapmap]
rs12300578	1.00[YRI][hapmap]
rs12305044	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12306906	1.00[EUR][1000 genomes]
rs12307540	0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12309121	1.00[EUR][1000 genomes]
rs12320150	1.00[EUR][1000 genomes]
rs1245433	1.00[EUR][1000 genomes]
rs1795213	1.00[EUR][1000 genomes]
rs3847912	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58600898	1.00[EUR][1000 genomes]
rs6581435	0.92[YRI][hapmap]
rs73310271	1.00[EUR][1000 genomes]
rs73310273	1.00[EUR][1000 genomes]
rs74096113	1.00[EUR][1000 genomes]
rs7962524	1.00[EUR][1000 genomes]
rs7964628	1.00[EUR][1000 genomes]
rs7977306	0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9738423	1.00[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	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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