Variant report

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

rs_ID	r²[population]
rs10259368	0.82[EUR][1000 genomes]
rs1528507	0.82[EUR][1000 genomes]
rs1528519	0.82[EUR][1000 genomes]
rs1528521	0.82[EUR][1000 genomes]
rs1585816	1.00[YRI][hapmap]
rs1819068	1.00[YRI][hapmap]
rs1950033	0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2286125	0.82[EUR][1000 genomes]
rs4725717	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4725736	0.87[EUR][1000 genomes]
rs4726854	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4726857	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4726858	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4726875	0.82[EUR][1000 genomes]
rs62481228	0.90[ASN][1000 genomes]
rs6464796	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6948780	0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7782445	0.85[EUR][1000 genomes]
rs7795712	0.82[EUR][1000 genomes]
rs7796028	0.86[EUR][1000 genomes]
rs7800366	0.85[EUR][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	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv608954	chr7:147104887-147145576	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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