Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:132982274..132985132-chr6:132986849..132988773,2	K562	blood:

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1024178	0.91[ASN][1000 genomes]
rs11962296	0.91[ASN][1000 genomes]
rs11965817	0.89[ASN][1000 genomes]
rs12174090	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1569652	0.91[ASN][1000 genomes]
rs1569653	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1569654	0.91[ASN][1000 genomes]
rs17061571	0.91[ASN][1000 genomes]
rs2064311	0.85[ASN][1000 genomes]
rs2064312	0.84[ASN][1000 genomes]
rs2267950	0.86[ASN][1000 genomes]
rs3798800	0.85[ASN][1000 genomes]
rs3798801	0.85[ASN][1000 genomes]
rs4435965	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4585585	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62425072	0.97[ASN][1000 genomes]
rs62425075	0.86[ASN][1000 genomes]
rs7747513	0.91[ASN][1000 genomes]
rs8192620	0.83[ASN][1000 genomes]
rs9321360	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9375903	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs9375906	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9375907	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9375911	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs9389022	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9389024	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9389025	0.86[ASN][1000 genomes]
rs9389026	0.86[ASN][1000 genomes]
rs9399037	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9399040	0.85[ASN][1000 genomes]
rs9402441	0.81[EUR][1000 genomes];0.83[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	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1015742	chr6:132933666-133285852	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 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	chr6:132985800-132987000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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