Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10011982	0.90[ASN][1000 genomes]
rs13119766	0.81[ASN][1000 genomes]
rs13127589	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13132576	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17055995	0.81[ASN][1000 genomes]
rs17730489	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28594344	0.81[ASN][1000 genomes]
rs34704211	0.81[ASN][1000 genomes]
rs34733312	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34998985	0.95[ASN][1000 genomes]
rs35270214	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35735782	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35988152	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3927277	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4123378	0.81[ASN][1000 genomes]
rs4591556	0.81[ASN][1000 genomes]
rs4607176	0.81[ASN][1000 genomes]
rs6855350	0.81[ASN][1000 genomes]
rs6855386	0.81[ASN][1000 genomes]
rs71607810	0.81[ASN][1000 genomes]
rs7667249	0.81[ASN][1000 genomes]
rs7667290	0.81[ASN][1000 genomes]
rs7672244	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[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	nsv596167	chr4:171576294-171672038	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv881141	chr4:171620514-171680223	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:171620400-171621800	Enhancers	GM12878-XiMat	blood
2	chr4:171620600-171620800	Enhancers	Aorta	Aorta

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