Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11012828	0.88[ASN][1000 genomes]
rs11012829	0.88[ASN][1000 genomes]
rs11012830	0.88[ASN][1000 genomes]
rs11012832	0.88[ASN][1000 genomes]
rs11012838	0.86[ASN][1000 genomes]
rs11012839	0.86[ASN][1000 genomes]
rs12572404	0.94[EUR][1000 genomes]
rs55822580	0.90[EUR][1000 genomes]
rs57831826	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58055243	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs60689569	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60858250	0.95[EUR][1000 genomes]
rs61545603	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61842423	0.85[AMR][1000 genomes]
rs61842424	0.90[AMR][1000 genomes]
rs61842425	0.82[AMR][1000 genomes]
rs61842428	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61842432	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61842437	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61842438	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61842440	0.85[AMR][1000 genomes]
rs74120238	0.84[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	nsv550039	chr10:18363924-18425519	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 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	chr10:18413200-18423400	Weak transcription	Fetal Heart	heart

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