Variant report

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

rs_ID	r²[population]
rs12587427	1.00[EUR][1000 genomes]
rs12588444	0.93[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs12590740	1.00[EUR][1000 genomes]
rs17107907	1.00[EUR][1000 genomes]
rs17107912	1.00[EUR][1000 genomes]
rs17107986	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17107993	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17108021	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17108073	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2287495	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57388154	0.87[EUR][1000 genomes]
rs58271165	1.00[EUR][1000 genomes]
rs58355788	0.88[ASN][1000 genomes]
rs60238041	0.87[EUR][1000 genomes]
rs60568650	0.87[EUR][1000 genomes]
rs7142533	1.00[EUR][1000 genomes]
rs7148807	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7153070	1.00[EUR][1000 genomes]
rs7153811	1.00[EUR][1000 genomes]
rs74064325	0.87[EUR][1000 genomes]
rs8012296	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2758363	chr14:78903610-79173528	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No data

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