Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:56304789..56307595-chr14:56316105..56318121,2	K562	blood:

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

rs_ID	r²[population]
rs11620875	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11621835	0.84[AMR][1000 genomes]
rs11624167	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11625869	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11626057	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs12890121	0.92[ASN][1000 genomes]
rs12894971	0.87[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs17832467	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2105058	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2152287	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs28490128	0.83[ASN][1000 genomes]
rs34096981	0.92[ASN][1000 genomes]
rs34540577	0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs34663121	0.93[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs35290945	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs35527253	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs36096896	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4601950	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs61975563	0.95[ASN][1000 genomes]
rs61975579	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs999817	0.88[AMR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901966	chr14:56160904-56436203	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv901977	chr14:56213392-56492996	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56305400-56311600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr14:56306200-56314800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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