Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10161731	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1017539	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11618497	0.81[EUR][1000 genomes]
rs1342669	0.81[EUR][1000 genomes]
rs1348466	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1373273	0.83[ASN][1000 genomes]
rs1373281	0.81[EUR][1000 genomes]
rs1443905	0.81[EUR][1000 genomes]
rs1443919	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1838278	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2165985	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2408860	0.94[ASN][1000 genomes]
rs7322098	0.83[ASN][1000 genomes]
rs7982022	0.80[EUR][1000 genomes]
rs7987501	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7997288	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7997746	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8001044	0.81[EUR][1000 genomes]
rs9316613	0.81[EUR][1000 genomes]
rs9536405	0.81[EUR][1000 genomes]
rs9536406	0.81[EUR][1000 genomes]
rs9596807	0.91[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	nsv1050969	chr13:53665927-54064861	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	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	chr13:54029400-54030200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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