Variant report

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

rs_ID	r²[population]
rs12106777	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1510366	0.82[ASN][1000 genomes]
rs1510367	0.82[ASN][1000 genomes]
rs17047687	0.82[ASN][1000 genomes]
rs17047694	0.82[ASN][1000 genomes]
rs17047725	0.82[ASN][1000 genomes]
rs2221758	0.82[ASN][1000 genomes]
rs262201	1.00[ASN][1000 genomes]
rs72626975	0.81[AMR][1000 genomes]
rs72626976	0.81[AMR][1000 genomes]
rs72626988	0.81[AMR][1000 genomes]
rs72626989	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs72626995	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72626996	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72626997	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72627000	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72627001	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72628614	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs72628615	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs957894	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834721	chr3:68365963-68526394	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv998582	chr3:68422687-68461190	Enhancers ZNF genes & repeats Active TSS 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	chr3:68435000-68435800	Enhancers	Adipose Nuclei	Adipose

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