Variant report

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

rs_ID	r²[population]
rs10399623	0.86[EUR][1000 genomes]
rs10889863	0.82[EUR][1000 genomes]
rs12059668	0.87[EUR][1000 genomes]
rs12063369	0.96[EUR][1000 genomes]
rs12086732	0.96[EUR][1000 genomes]
rs12090593	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12095499	1.00[CEU][hapmap]
rs17131037	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17131038	1.00[CEU][hapmap]
rs17131039	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17131047	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17131053	0.96[EUR][1000 genomes]
rs17131072	0.84[YRI][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2211659	0.84[YRI][hapmap]
rs61782560	0.96[EUR][1000 genomes]
rs61782572	0.96[EUR][1000 genomes]
rs61782573	0.96[EUR][1000 genomes]
rs61784020	0.84[EUR][1000 genomes]
rs61784021	0.84[EUR][1000 genomes]
rs61784023	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6695130	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67024201	0.83[AFR][1000 genomes]
rs72676804	0.81[EUR][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	nsv428466	chr1:70306638-70455357	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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