Variant report

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

rs_ID	r²[population]
rs11901852	0.86[ASN][1000 genomes]
rs1482838	0.95[ASN][1000 genomes]
rs17012034	0.90[ASN][1000 genomes]
rs17012037	0.90[ASN][1000 genomes]
rs17012041	1.00[ASN][1000 genomes]
rs17012116	0.85[ASN][1000 genomes]
rs4848263	0.82[ASN][1000 genomes]
rs55906816	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57373389	0.85[ASN][1000 genomes]
rs58960665	0.85[ASN][1000 genomes]
rs59648005	1.00[ASN][1000 genomes]
rs60413051	0.90[ASN][1000 genomes]
rs60659743	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6716689	1.00[ASN][1000 genomes]
rs6722936	1.00[AMR][1000 genomes]
rs72847374	0.82[ASN][1000 genomes]
rs73953210	0.90[ASN][1000 genomes]
rs73955824	0.94[AFR][1000 genomes]
rs73955828	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73955847	0.90[ASN][1000 genomes]
rs73955853	1.00[ASN][1000 genomes]
rs7605407	0.90[ASN][1000 genomes]
rs931241	1.00[AMR][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	nsv834360	chr2:125492685-125683200	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3384737	chr2:125587373-125587883	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:125580600-125591200	Weak transcription	Fetal Lung	lung

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