Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10099045	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12375320	0.99[ASN][1000 genomes]
rs12546239	0.81[ASN][1000 genomes]
rs12547877	0.99[ASN][1000 genomes]
rs12678112	0.81[ASN][1000 genomes]
rs16882264	0.94[ASN][1000 genomes]
rs2028776	0.96[ASN][1000 genomes]
rs2044355	0.90[EUR][1000 genomes]
rs2166231	0.90[EUR][1000 genomes]
rs28503648	0.96[ASN][1000 genomes]
rs28545279	0.94[ASN][1000 genomes]
rs2896967	0.89[EUR][1000 genomes]
rs4739565	0.89[ASN][1000 genomes]
rs55752257	0.99[ASN][1000 genomes]
rs55849895	0.81[ASN][1000 genomes]
rs56355533	0.87[ASN][1000 genomes]
rs59516528	0.89[ASN][1000 genomes]
rs6468262	0.99[ASN][1000 genomes]
rs6993906	0.81[ASN][1000 genomes]
rs7012499	0.99[ASN][1000 genomes]
rs7464162	0.89[ASN][1000 genomes]
rs7815684	0.81[ASN][1000 genomes]
rs7816886	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7827467	0.99[ASN][1000 genomes]
rs7833514	0.90[EUR][1000 genomes]
rs7834257	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7836137	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9297220	0.90[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	nsv6147	chr8:34314029-34359124	Weak transcription Enhancers	Chromatin interactive region	2 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	chr8:34338600-34340200	Enhancers	Fetal Kidney	kidney

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