Variant report

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

rs_ID	r²[population]
rs12053661	0.87[AMR][1000 genomes]
rs12053685	0.87[AMR][1000 genomes]
rs13051727	0.91[ASN][1000 genomes]
rs13433511	0.91[ASN][1000 genomes]
rs1569338	0.91[ASN][1000 genomes]
rs17241011	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17306721	0.93[ASN][1000 genomes]
rs2094859	0.91[AMR][1000 genomes]
rs2822939	0.90[ASN][1000 genomes]
rs2822941	0.90[ASN][1000 genomes]
rs2822942	0.93[ASN][1000 genomes]
rs2822943	0.84[ASN][1000 genomes]
rs2822944	0.93[ASN][1000 genomes]
rs2822945	0.93[ASN][1000 genomes]
rs2822948	0.96[ASN][1000 genomes]
rs2822949	0.94[ASN][1000 genomes]
rs2822951	0.96[ASN][1000 genomes]
rs2822954	1.00[ASN][1000 genomes]
rs2822955	0.97[ASN][1000 genomes]
rs34352557	0.93[ASN][1000 genomes]
rs35937945	0.89[ASN][1000 genomes]
rs57530452	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59113791	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61161554	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62219731	0.90[ASN][1000 genomes]
rs62219732	0.93[ASN][1000 genomes]
rs7277621	1.00[ASN][1000 genomes]
rs7281621	1.00[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	nsv869911	chr21:16184645-16210579	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16199200-16204600	Weak transcription	K562	blood

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