Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10857114	0.89[AMR][1000 genomes]
rs11098875	0.89[AMR][1000 genomes]
rs11098877	0.89[AMR][1000 genomes]
rs11098878	0.88[ASN][1000 genomes]
rs11098881	0.86[ASN][1000 genomes]
rs11098882	0.86[ASN][1000 genomes]
rs12498989	0.89[AMR][1000 genomes]
rs12501073	0.89[AMR][1000 genomes]
rs12641163	0.89[AMR][1000 genomes]
rs12643879	0.89[AMR][1000 genomes]
rs12650060	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28558216	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56358919	0.85[ASN][1000 genomes]
rs58302722	0.88[ASN][1000 genomes]
rs59819551	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61193656	0.89[AMR][1000 genomes]
rs61359035	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7687335	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7687529	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7687807	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7687848	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7691736	0.95[EUR][1000 genomes];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	nsv595385	chr4:127383473-127451806	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127417000-127419800	Weak transcription	K562	blood

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