Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10734533	0.86[ASN][1000 genomes]
rs10838492	0.84[ASN][1000 genomes]
rs12574417	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12574431	0.94[ASN][1000 genomes]
rs12575810	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12576823	0.86[ASN][1000 genomes]
rs12577157	0.86[ASN][1000 genomes]
rs12577749	0.81[ASN][1000 genomes]
rs1374750	0.84[ASN][1000 genomes]
rs1562458	0.84[ASN][1000 genomes]
rs1562459	0.86[ASN][1000 genomes]
rs17195752	0.91[ASN][1000 genomes]
rs17195773	0.91[ASN][1000 genomes]
rs35198848	0.86[ASN][1000 genomes]
rs55989803	0.94[ASN][1000 genomes]
rs57159413	0.80[ASN][1000 genomes]
rs60227611	0.91[ASN][1000 genomes]
rs60865673	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs72899266	0.91[ASN][1000 genomes]
rs72899277	0.91[ASN][1000 genomes]
rs72899286	0.91[ASN][1000 genomes]
rs72901205	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72904962	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72904977	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72904985	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72910637	0.86[ASN][1000 genomes]
rs72910671	0.85[AMR][1000 genomes];0.87[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	nsv897310	chr11:45487041-45631953	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr11:45615000-45626200	Weak transcription	Fetal Brain Male	brain

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