Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1146079	0.83[JPT][hapmap]
rs191551	0.91[JPT][hapmap]
rs2951468	0.95[CEU][hapmap]
rs2951531	0.91[JPT][hapmap]
rs348635	0.91[JPT][hapmap]
rs348636	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs348638	0.81[JPT][hapmap]
rs348639	0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs348652	0.83[JPT][hapmap]
rs348654	0.83[JPT][hapmap]
rs348655	0.90[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs348660	0.90[JPT][hapmap]
rs348661	0.89[JPT][hapmap]
rs348662	0.91[JPT][hapmap]
rs348663	0.91[JPT][hapmap]
rs348664	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs348672	0.83[JPT][hapmap]
rs348675	0.81[JPT][hapmap]
rs348676	0.83[JPT][hapmap]
rs348679	0.81[JPT][hapmap]
rs348686	1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs348692	1.00[CEU][hapmap];0.91[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs348695	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs348696	0.81[CEU][hapmap];0.83[EUR][1000 genomes]
rs980891	0.81[CEU][hapmap];0.82[AFR][1000 genomes];0.80[EUR][1000 genomes]

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	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62422600-62429000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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