Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1116556	0.99[AFR][1000 genomes];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1116557	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2148919	0.93[EUR][1000 genomes]
rs2148920	0.95[EUR][1000 genomes]
rs2148921	0.95[EUR][1000 genomes]
rs2148922	0.95[EUR][1000 genomes]
rs2148923	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2896874	0.85[EUR][1000 genomes]
rs4999222	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6036177	0.94[EUR][1000 genomes]
rs6036178	0.93[EUR][1000 genomes]
rs6036192	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6036194	0.83[EUR][1000 genomes]
rs6048268	0.92[EUR][1000 genomes]
rs6048269	0.92[EUR][1000 genomes]
rs6075938	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6075944	0.87[EUR][1000 genomes]
rs6082792	0.93[EUR][1000 genomes]
rs6082793	0.85[EUR][1000 genomes]
rs6082797	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6132541	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6132542	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6132543	0.85[EUR][1000 genomes]
rs6137726	0.81[EUR][1000 genomes]
rs6137727	0.80[EUR][1000 genomes]
rs6137731	0.89[AFR][1000 genomes]
rs6137732	0.86[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	nsv833943	chr20:22657016-22703454	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 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	chr20:22687200-22697400	Weak transcription	Aorta	Aorta

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