Variant report

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

rs_ID	r²[population]
rs11726385	0.84[ASN][1000 genomes]
rs11728322	0.95[ASN][1000 genomes]
rs1426936	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17052159	0.95[ASN][1000 genomes]
rs17052161	0.95[ASN][1000 genomes]
rs17052168	0.85[ASN][1000 genomes]
rs2195039	0.95[ASN][1000 genomes]
rs2332896	0.94[ASN][1000 genomes]
rs2332898	0.85[ASN][1000 genomes]
rs35549890	0.85[ASN][1000 genomes]
rs35780342	0.85[ASN][1000 genomes]
rs36112171	0.92[ASN][1000 genomes]
rs4147100	0.85[ASN][1000 genomes]
rs5012181	0.94[ASN][1000 genomes]
rs59300323	0.95[ASN][1000 genomes]
rs62337142	0.95[ASN][1000 genomes]
rs62337145	0.93[ASN][1000 genomes]
rs62337147	0.85[ASN][1000 genomes]
rs62337155	0.85[ASN][1000 genomes]
rs6827776	0.93[ASN][1000 genomes]
rs7682749	0.85[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	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 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	chr4:175383600-175388200	Weak transcription	Muscle Satellite Cultured Cells	--

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