Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11119654	0.81[AFR][1000 genomes]
rs12022715	0.81[AFR][1000 genomes]
rs12022739	0.81[AFR][1000 genomes]
rs12042686	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12043937	0.80[AFR][1000 genomes]
rs12043952	0.80[AFR][1000 genomes]
rs12070402	0.81[AFR][1000 genomes]
rs12406562	0.97[AFR][1000 genomes]
rs1501548	0.80[AFR][1000 genomes]
rs1501549	0.81[AFR][1000 genomes]
rs1501550	0.81[AFR][1000 genomes]
rs1501557	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1532682	0.81[AFR][1000 genomes]
rs4951693	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4951695	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6689715	0.81[AFR][1000 genomes]
rs7524268	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7526579	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7551412	0.86[AFR][1000 genomes]
rs7553997	0.97[AFR][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	esv3437481	chr1:211139629-211143927	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211123000-211152000	Weak transcription	HSMM	muscle

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