Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10784287	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10877804	0.95[CHB][hapmap];0.83[ASN][1000 genomes]
rs10877817	0.86[ASN][1000 genomes]
rs11174358	1.00[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs11174360	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11174361	0.80[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11174368	0.95[ASN][1000 genomes]
rs11174369	0.96[ASN][1000 genomes]
rs11174373	0.94[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs11174377	0.87[ASN][1000 genomes]
rs11174378	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs11174383	0.81[ASN][1000 genomes]
rs12823493	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1406799	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1920087	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1920096	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs2884779	0.90[CHB][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap]
rs3759290	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7305206	0.82[CHB][hapmap]
rs7305482	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7308544	0.81[ASN][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	nsv832435	chr12:62407000-62601835	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62568800-62581800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr12:62578600-62581800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:62579200-62580000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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