Variant report

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10084437	0.82[CHB][hapmap]
rs10166480	0.82[CHB][hapmap]
rs10178842	0.82[CHB][hapmap]
rs10179213	0.82[CHB][hapmap]
rs10183674	0.82[CHB][hapmap]
rs10184800	0.82[CHB][hapmap]
rs10185492	0.82[CHB][hapmap]
rs10208814	0.82[CHB][hapmap]
rs11123062	0.82[CHB][hapmap]
rs11680115	0.82[CHB][hapmap]
rs11684422	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12468133	0.82[CHB][hapmap]
rs12469969	0.82[CHB][hapmap]
rs12623831	0.82[CHB][hapmap]
rs13003204	0.82[CHB][hapmap]
rs13021629	1.00[CHB][hapmap]
rs13396871	0.82[CHB][hapmap]
rs13400133	0.82[CHB][hapmap]
rs13409512	0.82[CHB][hapmap]
rs13427244	0.82[CHB][hapmap]
rs1586081	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17393599	0.82[CHB][hapmap]
rs4848259	0.82[CHB][hapmap]
rs62171305	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6713505	0.82[CHB][hapmap]
rs6736347	0.82[CHB][hapmap]
rs6760383	0.82[CHB][hapmap]
rs717601	0.82[CHB][hapmap]
rs730468	0.82[CHB][hapmap]
rs7560538	0.82[CHB][hapmap]
rs7582461	0.82[CHB][hapmap]
rs7584662	0.82[CHB][hapmap]
rs7588987	0.82[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834359	chr2:125367872-125536022	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
2	nsv428727	chr2:125372897-125512949	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island	1 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	chr2:125455600-125460000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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