Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10248165	0.89[ASN][1000 genomes]
rs10251013	0.83[ASN][1000 genomes]
rs10269183	0.88[ASN][1000 genomes]
rs10951603	0.84[ASN][1000 genomes]
rs11971775	0.97[ASN][1000 genomes]
rs1558159	0.83[ASN][1000 genomes]
rs1990243	0.99[ASN][1000 genomes]
rs2190887	0.82[ASN][1000 genomes]
rs2237411	0.82[ASN][1000 genomes]
rs2299135	0.97[ASN][1000 genomes]
rs2299137	0.85[ASN][1000 genomes]
rs2299140	0.83[ASN][1000 genomes]
rs2299141	0.83[ASN][1000 genomes]
rs2329388	0.83[ASN][1000 genomes]
rs2329389	0.83[ASN][1000 genomes]
rs2329390	0.83[ASN][1000 genomes]
rs2329391	0.83[ASN][1000 genomes]
rs2876835	0.95[ASN][1000 genomes]
rs3800854	0.83[ASN][1000 genomes]
rs60586729	0.99[ASN][1000 genomes]
rs6962623	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs740509	0.85[ASN][1000 genomes]
rs917401	0.89[ASN][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	nsv1021180	chr7:39424988-39642261	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39426000-39432800	Weak transcription	Fetal Muscle Leg	muscle

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