Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10166875	0.91[EUR][1000 genomes]
rs10169970	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10183152	0.97[EUR][1000 genomes]
rs17335518	0.88[EUR][1000 genomes]
rs1851169	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1851170	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1983399	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2371308	0.96[EUR][1000 genomes]
rs4016512	0.97[EUR][1000 genomes]
rs4673628	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62185367	0.88[EUR][1000 genomes]
rs6714837	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6741480	0.98[EUR][1000 genomes]
rs6743138	0.98[EUR][1000 genomes]
rs6755268	0.98[EUR][1000 genomes]
rs7562364	0.97[EUR][1000 genomes]
rs7562573	0.97[EUR][1000 genomes]
rs7565321	0.92[EUR][1000 genomes]
rs7565327	0.98[EUR][1000 genomes]
rs7579224	0.91[EUR][1000 genomes]
rs7591647	0.98[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	nsv875783	chr2:212530466-212564895	Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region	1 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	chr2:212547200-212568600	Weak transcription	Fetal Kidney	kidney

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