Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10099045	0.94[ASN][1000 genomes]
rs10100459	0.94[ASN][1000 genomes]
rs12375320	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12546239	0.83[ASN][1000 genomes]
rs12547877	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12678112	0.83[ASN][1000 genomes]
rs16882264	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16882360	0.86[EUR][1000 genomes]
rs2028776	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28366982	0.86[EUR][1000 genomes]
rs28503648	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4739565	0.86[ASN][1000 genomes]
rs55752257	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55849895	0.83[ASN][1000 genomes]
rs56355533	0.85[ASN][1000 genomes]
rs59516528	0.86[ASN][1000 genomes]
rs6468262	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6993906	0.83[ASN][1000 genomes]
rs7012499	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7464162	0.86[ASN][1000 genomes]
rs7815684	0.83[ASN][1000 genomes]
rs7816886	0.90[ASN][1000 genomes]
rs7827467	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7834257	0.90[ASN][1000 genomes]
rs7836137	0.90[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	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	chr8:34356200-34356600	Enhancers	Fetal Heart	heart

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