Variant report

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

rs_ID	r²[population]
rs10004125	0.83[ASN][1000 genomes]
rs10016914	1.00[ASN][1000 genomes]
rs10020515	1.00[ASN][1000 genomes]
rs10155080	0.94[ASN][1000 genomes]
rs1320227	0.83[ASN][1000 genomes]
rs13340296	0.83[ASN][1000 genomes]
rs17631460	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17631610	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2139210	0.81[ASN][1000 genomes]
rs28360736	0.92[ASN][1000 genomes]
rs28435653	0.94[ASN][1000 genomes]
rs4270546	0.81[ASN][1000 genomes]
rs4515120	0.82[ASN][1000 genomes]
rs4691203	1.00[ASN][1000 genomes]
rs59998429	0.83[ASN][1000 genomes]
rs67582214	0.83[ASN][1000 genomes]
rs6821186	0.83[ASN][1000 genomes]
rs6854385	0.83[ASN][1000 genomes]
rs72705432	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72705435	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7440432	0.83[ASN][1000 genomes]
rs7672909	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7696979	0.92[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	nsv596052	chr4:166454826-166488615	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription	TF binding region 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	chr4:166482600-166484200	Weak transcription	Osteobl	bone
2	chr4:166483200-166485000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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