Variant report

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

rs_ID	r²[population]
rs10218858	0.84[AFR][1000 genomes]
rs10740127	0.88[ASN][1000 genomes]
rs10761774	0.95[ASN][1000 genomes]
rs10995547	0.80[AFR][1000 genomes]
rs2660199	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2660200	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2660201	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2666536	0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2666545	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2666546	0.95[ASN][1000 genomes]
rs2666547	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2879546	0.84[AFR][1000 genomes]
rs4542348	0.82[AFR][1000 genomes]
rs4576762	0.94[ASN][1000 genomes]
rs4935009	0.95[ASN][1000 genomes]
rs4935218	0.95[ASN][1000 genomes]
rs7073617	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7074981	0.88[ASN][1000 genomes]
rs7091200	0.80[EUR][1000 genomes]
rs7476747	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831873	chr10:52710610-52899540	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv895394	chr10:52793177-52866503	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1036645	chr10:52804961-53159076	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 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	chr10:52807600-52821000	Weak transcription	Aorta	Aorta

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