Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10467248	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11839229	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11839416	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11839791	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11841051	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12584695	1.00[EUR][1000 genomes]
rs12585540	1.00[EUR][1000 genomes]
rs13378556	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16951689	1.00[EUR][1000 genomes]
rs16953167	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57699320	0.83[EUR][1000 genomes]
rs58265487	0.83[AFR][1000 genomes]
rs58482261	0.84[AFR][1000 genomes]
rs60510396	0.83[AFR][1000 genomes]
rs67787923	0.92[AFR][1000 genomes]
rs7337357	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73552169	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9302073	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9302085	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9590167	0.86[AFR][1000 genomes]
rs9590170	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9590326	0.86[AFR][1000 genomes]
rs961862	0.84[AFR][1000 genomes]
rs9805799	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[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	nsv1047136	chr13:86979109-87555131	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2763045	chr13:87005617-87079364	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:87004600-87009800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr13:87005800-87008000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr13:87006400-87007000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr13:87006400-87007600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr13:87006600-87011200	Weak transcription	H9 Cell Line	embryonic stem cell

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