Variant report

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

rs_ID	r²[population]
rs11123018	0.98[ASN][1000 genomes]
rs11679532	0.87[AFR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11679636	0.82[AFR][1000 genomes]
rs11896878	0.95[CEU][hapmap]
rs12465377	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12475898	0.95[CEU][hapmap]
rs13032868	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1347875	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1439134	0.83[AFR][1000 genomes]
rs1439135	0.95[CEU][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17271252	0.90[CEU][hapmap]
rs17271568	0.95[CEU][hapmap]
rs1866479	0.95[CEU][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2420439	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2420441	0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs3902861	0.95[CEU][hapmap]
rs4340523	0.81[AFR][1000 genomes]
rs4362567	0.85[EUR][1000 genomes]
rs4588195	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6746702	1.00[CEU][hapmap]
rs7566987	0.85[CEU][hapmap]
rs951032	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs980374	0.95[CEU][hapmap]

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	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No data

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