Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10014805	0.80[EUR][1000 genomes]
rs10015002	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10017564	0.86[EUR][1000 genomes]
rs10021157	0.86[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs10025078	0.81[EUR][1000 genomes]
rs12503113	0.86[EUR][1000 genomes]
rs12506489	0.86[EUR][1000 genomes]
rs12506702	0.86[EUR][1000 genomes]
rs12510173	0.86[EUR][1000 genomes]
rs12640600	0.86[EUR][1000 genomes]
rs1860129	0.84[EUR][1000 genomes]
rs2190907	0.84[EUR][1000 genomes]
rs2237040	0.81[EUR][1000 genomes]
rs2282784	0.86[EUR][1000 genomes]
rs2298978	0.86[EUR][1000 genomes]
rs2298979	0.86[EUR][1000 genomes]
rs2298983	0.85[EUR][1000 genomes]
rs2347137	0.84[EUR][1000 genomes]
rs2881559	0.86[EUR][1000 genomes]
rs3796944	0.86[EUR][1000 genomes]
rs3796948	0.85[EUR][1000 genomes]
rs4444903	0.88[EUR][1000 genomes]
rs6533482	0.85[EUR][1000 genomes]
rs6533483	0.84[EUR][1000 genomes]
rs6855847	0.84[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs882405	0.86[EUR][1000 genomes]
rs929446	0.84[EUR][1000 genomes]
rs9994491	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[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	nsv530156	chr4:110721397-110911297	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr4:110825000-110834000	Weak transcription	Psoas Muscle	Psoas

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