Variant report

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

rs_ID	r²[population]
rs11710516	0.82[ASW][hapmap]
rs182936	0.82[ASW][hapmap]
rs4474996	1.00[ASW][hapmap];0.86[YRI][hapmap]
rs58895069	0.93[AFR][1000 genomes]
rs59980662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6441097	1.00[ASW][hapmap];0.95[LWK][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes]
rs6441098	0.86[YRI][hapmap]
rs6783490	0.93[YRI][hapmap]
rs6798879	0.84[YRI][hapmap]
rs6807765	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs73873737	0.81[AFR][1000 genomes]
rs7638335	0.93[YRI][hapmap];0.81[AFR][1000 genomes]
rs9289974	0.93[YRI][hapmap]
rs9809108	0.93[YRI][hapmap];0.81[AFR][1000 genomes]
rs9814973	0.84[AFR][1000 genomes]
rs9831523	1.00[YRI][hapmap]
rs9836414	0.90[ASW][hapmap];0.85[LWK][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs9850381	0.86[YRI][hapmap]
rs9862136	1.00[AFR][1000 genomes]
rs9865537	1.00[YRI][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	nsv829765	chr3:156568263-156718496	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv592120	chr3:156626091-156691604	Enhancers Weak transcription Strong transcription Flanking 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	chr3:156675200-156676400	Flanking Active TSS	GM12878-XiMat	blood

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