Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10170802	0.94[EUR][1000 genomes]
rs12473082	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1404085	1.00[AFR][1000 genomes]
rs1404088	1.00[AFR][1000 genomes]
rs1524216	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1533985	1.00[AFR][1000 genomes]
rs1554617	1.00[AFR][1000 genomes]
rs1554618	1.00[AFR][1000 genomes]
rs1608586	0.94[EUR][1000 genomes]
rs1660568	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2083550	0.94[EUR][1000 genomes]
rs2901742	0.94[EUR][1000 genomes]
rs2901743	1.00[AFR][1000 genomes]
rs317288	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs317290	0.91[EUR][1000 genomes]
rs390810	0.94[EUR][1000 genomes]
rs393801	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs414148	1.00[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs421370	1.00[ASN][1000 genomes]
rs425915	0.94[EUR][1000 genomes]
rs426141	1.00[ASN][1000 genomes]
rs449418	0.94[EUR][1000 genomes]
rs4640412	0.94[EUR][1000 genomes]
rs6753413	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6759874	0.94[EUR][1000 genomes]
rs7576329	1.00[AFR][1000 genomes]
rs7589273	1.00[AFR][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	nsv834265	chr2:76275611-76450728	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:76300400-76302600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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