Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:71424613..71426717-chr16:71432993..71434718,2	K562	blood:

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11075886	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11075887	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12373064	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12373108	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12595924	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12597011	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12597949	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12927445	0.82[ASN][1000 genomes]
rs34623821	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34659305	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34770624	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35060794	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35097873	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35886140	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4488452	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57243109	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72789961	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72789969	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7498368	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8051854	0.83[ASN][1000 genomes]
rs8052248	0.83[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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71424200-71436000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:71432600-71434400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr16:71433200-71434400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr16:71433800-71435000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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