Variant report

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

rs_ID	r²[population]
rs11075886	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11075887	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12373064	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12373108	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12596074	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12597011	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12597949	0.82[AMR][1000 genomes]
rs12927445	0.86[ASN][1000 genomes]
rs34585976	0.80[AMR][1000 genomes]
rs34623821	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34659305	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34770624	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35060794	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35097873	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35886140	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4488452	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57243109	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72789961	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72789969	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7498368	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8051854	0.86[ASN][1000 genomes]
rs8052248	0.86[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	nsv949461	chr16:71196153-71579711	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 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	chr16:71434800-71446600	Weak transcription	Right Atrium	heart
2	chr16:71436600-71438600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:71436600-71446000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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