Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10084437	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10166480	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10177603	1.00[YRI][hapmap]
rs12469969	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12612581	0.82[CHB][hapmap]
rs13003204	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13432413	0.82[YRI][hapmap]
rs17393599	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2123855	0.96[YRI][hapmap]
rs2168024	1.00[YRI][hapmap]
rs4848260	1.00[CEU][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62171336	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62171337	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6739209	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6739388	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7560538	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7584662	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7588987	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs961459	1.00[YRI][hapmap]
rs962200	0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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
3	nsv834360	chr2:125492685-125683200	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	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	chr2:125511000-125511800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

Quick Search: