Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10139152	0.83[ASN][1000 genomes]
rs10149999	0.83[ASN][1000 genomes]
rs10151794	0.83[ASN][1000 genomes]
rs11620910	0.89[EUR][1000 genomes]
rs11624616	0.93[EUR][1000 genomes]
rs12323598	0.87[EUR][1000 genomes]
rs17110868	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55859597	0.83[ASN][1000 genomes]
rs57289554	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs57315708	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57759210	0.87[EUR][1000 genomes]
rs61391568	0.87[EUR][1000 genomes]
rs6574591	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7151041	1.00[ASN][1000 genomes]
rs7156847	0.93[EUR][1000 genomes]
rs7157244	0.93[EUR][1000 genomes]
rs7159335	0.93[EUR][1000 genomes]
rs73330519	0.83[ASN][1000 genomes]
rs73330520	0.83[ASN][1000 genomes]
rs74066058	1.00[ASN][1000 genomes]
rs8008763	0.91[EUR][1000 genomes]
rs8014976	0.93[EUR][1000 genomes]
rs8016841	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8017020	0.82[AMR][1000 genomes];0.93[EUR][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	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr14:81076200-81086600	Weak transcription	A549	lung
2	chr14:81082200-81083400	Enhancers	Dnd41	blood

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