Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs16928580	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16928599	1.00[ASN][1000 genomes]
rs17237587	1.00[ASN][1000 genomes]
rs17810421	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59158455	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60099345	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61214522	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7007348	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72649311	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72649343	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72666305	0.86[EUR][1000 genomes]
rs72666306	0.86[EUR][1000 genomes]
rs72666307	0.86[EUR][1000 genomes]
rs72666308	0.86[EUR][1000 genomes]
rs72666309	0.86[EUR][1000 genomes]
rs72666310	0.83[EUR][1000 genomes]
rs72666317	0.86[EUR][1000 genomes]
rs72666319	0.86[EUR][1000 genomes]
rs72666321	0.86[EUR][1000 genomes]
rs7821022	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[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	nsv890955	chr8:62919691-63062581	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr8:63044600-63045400	Enhancers	A549	lung

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