Variant report

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs12662965	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12664024	0.89[ASN][1000 genomes]
rs1350943	0.93[ASN][1000 genomes]
rs1350944	0.93[ASN][1000 genomes]
rs1381688	0.93[ASN][1000 genomes]
rs1462491	0.93[ASN][1000 genomes]
rs56662730	0.90[ASN][1000 genomes]
rs6568630	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6922536	0.90[ASN][1000 genomes]
rs73533811	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73765657	0.93[ASN][1000 genomes]
rs73765660	0.92[ASN][1000 genomes]
rs7752069	0.90[ASN][1000 genomes]
rs7770634	0.93[ASN][1000 genomes]
rs9374149	0.99[ASN][1000 genomes]
rs9374151	0.96[ASN][1000 genomes]
rs9374152	0.93[ASN][1000 genomes]
rs9374153	0.90[ASN][1000 genomes]
rs9374154	0.93[ASN][1000 genomes]
rs9374155	0.90[ASN][1000 genomes]
rs9374157	0.90[ASN][1000 genomes]
rs9384733	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9386871	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9386873	0.99[ASN][1000 genomes]
rs9386874	0.99[ASN][1000 genomes]
rs9386875	0.99[ASN][1000 genomes]
rs9386877	0.90[ASN][1000 genomes]
rs9386878	0.90[ASN][1000 genomes]
rs9386879	0.90[ASN][1000 genomes]
rs9398230	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9400356	0.94[ASN][1000 genomes]
rs9400357	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9400358	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9400361	0.90[ASN][1000 genomes]
rs9400362	0.90[ASN][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	nsv1017642	chr6:110252276-110386453	Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv538417	chr6:110252276-110386453	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110371600-110374600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr6:110372400-110373800	Enhancers	Primary neutrophils fromperipheralblood	blood

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