Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10851861	0.88[EUR][1000 genomes]
rs11072395	0.88[EUR][1000 genomes]
rs11631402	0.92[EUR][1000 genomes]
rs11632408	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11636130	0.92[EUR][1000 genomes]
rs11638999	0.88[EUR][1000 genomes]
rs11852401	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11854040	0.92[EUR][1000 genomes]
rs11857236	0.92[EUR][1000 genomes]
rs12148518	0.92[EUR][1000 genomes]
rs12441946	0.89[EUR][1000 genomes]
rs1449266	0.89[EUR][1000 genomes]
rs1449269	0.89[EUR][1000 genomes]
rs1839270	0.89[EUR][1000 genomes]
rs1868473	0.90[EUR][1000 genomes]
rs2100202	0.92[EUR][1000 genomes]
rs2100203	0.89[EUR][1000 genomes]
rs2197893	0.92[EUR][1000 genomes]
rs2197894	0.92[EUR][1000 genomes]
rs28647497	0.92[EUR][1000 genomes]
rs4315307	0.89[EUR][1000 genomes]
rs4776618	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62016086	0.92[EUR][1000 genomes]
rs71397270	0.82[EUR][1000 genomes]
rs8028981	0.92[EUR][1000 genomes]
rs8041735	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][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	esv3352103	chr15:73191535-73454001	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr15:73212000-73213800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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