Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:67804547..67807310-chr13:67807944..67812554,4	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1325678	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1925750	0.84[ASN][1000 genomes]
rs1983871	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2147998	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2182229	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2325025	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2325027	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3812859	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3812860	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71427643	0.83[ASN][1000 genomes]
rs7489531	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7992750	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8002263	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9317651	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9529206	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9541034	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9541035	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9541039	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9541041	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9571740	0.86[EUR][1000 genomes];0.84[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	nsv1035741	chr13:67212973-68077950	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv541817	chr13:67212973-68077950	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr13:67809600-67812800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr13:67810800-67811600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr13:67810800-67811600	Active TSS	Right Atrium	heart
4	chr13:67811000-67811600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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