Variant report

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

rs_ID	r²[population]
rs17106669	0.85[EUR][1000 genomes]
rs34370136	0.85[EUR][1000 genomes]
rs34821441	0.85[EUR][1000 genomes]
rs35286623	0.89[EUR][1000 genomes]
rs35596448	0.91[EUR][1000 genomes]
rs55934143	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56014839	0.85[EUR][1000 genomes]
rs56378211	0.85[EUR][1000 genomes]
rs72814147	0.80[EUR][1000 genomes]
rs72814166	0.85[EUR][1000 genomes]
rs72814183	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72814184	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72814186	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72814188	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72814190	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72814201	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72814202	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72816104	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72816109	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72816113	1.00[AMR][1000 genomes];1.00[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	nsv551837	chr10:89707265-89777788	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:89758400-89785800	Weak transcription	Aorta	Aorta
2	chr10:89773000-89777400	Weak transcription	NHDF-Ad	bronchial
3	chr10:89774200-89785600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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