Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10865645	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11128114	1.00[ASN][1000 genomes]
rs11719988	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17005393	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs28591428	0.93[ASN][1000 genomes]
rs34890270	0.93[ASN][1000 genomes]
rs4241384	0.98[ASN][1000 genomes]
rs4241395	0.94[ASN][1000 genomes]
rs4389485	0.95[ASN][1000 genomes]
rs4407408	0.94[ASN][1000 genomes]
rs4425262	0.98[ASN][1000 genomes]
rs4461426	1.00[ASN][1000 genomes]
rs4504171	1.00[ASN][1000 genomes]
rs4522769	1.00[ASN][1000 genomes]
rs4560302	1.00[ASN][1000 genomes]
rs4563416	1.00[ASN][1000 genomes]
rs4563417	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4589943	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4621333	1.00[ASN][1000 genomes]
rs6792358	1.00[ASN][1000 genomes]
rs72924889	0.91[ASN][1000 genomes]
rs72924892	0.94[ASN][1000 genomes]
rs9883017	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	nsv876933	chr3:69059023-69227379	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 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	chr3:69194400-69200600	Weak transcription	Psoas Muscle	Psoas

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