Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs13067024	1.00[ASN][1000 genomes]
rs28441035	0.83[ASN][1000 genomes]
rs28617316	0.83[ASN][1000 genomes]
rs28619078	0.84[ASN][1000 genomes]
rs34971719	1.00[ASN][1000 genomes]
rs6550742	0.83[ASN][1000 genomes]
rs73033541	0.81[AMR][1000 genomes]
rs73040063	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73040065	0.82[EUR][1000 genomes]
rs73040067	0.82[EUR][1000 genomes]
rs73040068	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73042198	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73044320	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73050239	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73050248	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73050286	0.84[ASN][1000 genomes]
rs73050291	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7619223	0.99[ASN][1000 genomes]
rs7640945	0.99[ASN][1000 genomes]
rs9817417	0.83[ASN][1000 genomes]
rs9817740	0.83[ASN][1000 genomes]
rs9822814	0.83[ASN][1000 genomes]
rs9859793	1.00[ASN][1000 genomes]
rs9870844	0.83[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	nsv999882	chr3:23121533-23257718	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv834636	chr3:23138653-23301443	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr3:23216000-23217800	Enhancers	HUVEC	blood vessel

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