Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1329825	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1571545	0.84[ASN][1000 genomes]
rs16997384	0.87[ASN][1000 genomes]
rs16997388	0.89[ASN][1000 genomes]
rs16997391	0.91[ASN][1000 genomes]
rs2327986	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2876423	0.98[ASN][1000 genomes]
rs4814459	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4814460	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59809424	0.81[ASN][1000 genomes]
rs6034418	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6034424	0.99[ASN][1000 genomes]
rs6043822	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6043823	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6043824	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6514666	0.87[ASN][1000 genomes]
rs73898449	0.81[ASN][1000 genomes]
rs73898450	0.81[ASN][1000 genomes]
rs8118036	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9784173	0.91[ASN][1000 genomes]
rs9784178	0.91[ASN][1000 genomes]
rs9784181	0.91[ASN][1000 genomes]
rs9784187	0.91[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	nsv833930	chr20:16134347-16302763	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 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	chr20:16234200-16235000	Enhancers	Fetal Heart	heart

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