Variant report

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

rs_ID	r²[population]
rs10225178	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10237275	0.81[EUR][1000 genomes]
rs10252729	0.81[EUR][1000 genomes]
rs10254471	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10265230	0.85[ASN][1000 genomes]
rs12706272	0.80[ASN][1000 genomes]
rs17142585	0.81[EUR][1000 genomes]
rs2190183	0.81[EUR][1000 genomes]
rs2190184	0.85[EUR][1000 genomes]
rs58778277	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60578704	0.82[EUR][1000 genomes]
rs61273762	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62469500	0.86[ASN][1000 genomes]
rs62469501	0.86[ASN][1000 genomes]
rs62477431	0.80[ASN][1000 genomes]
rs6943223	0.81[EUR][1000 genomes]
rs6961750	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6974349	0.81[EUR][1000 genomes]
rs73213448	0.86[ASN][1000 genomes]
rs7777091	0.86[ASN][1000 genomes]
rs7786492	0.86[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	nsv831113	chr7:119683515-119886277	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	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	chr7:119800000-119801000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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