Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10734348	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10742016	1.00[ASN][1000 genomes]
rs10742017	1.00[ASN][1000 genomes]
rs10767140	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10767142	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10767144	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10834250	1.00[ASN][1000 genomes]
rs11027626	0.83[ASN][1000 genomes]
rs12288059	0.83[ASN][1000 genomes]
rs12290166	0.83[ASN][1000 genomes]
rs1879229	1.00[ASN][1000 genomes]
rs1919220	1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2037833	1.00[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2139513	1.00[ASN][1000 genomes]
rs2896682	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2946785	1.00[ASN][1000 genomes]
rs2946786	1.00[ASN][1000 genomes]
rs3992999	1.00[ASN][1000 genomes]
rs4287336	1.00[ASN][1000 genomes]
rs4385898	1.00[ASN][1000 genomes]
rs4396287	1.00[ASN][1000 genomes]
rs4547089	1.00[ASN][1000 genomes]
rs4922669	1.00[ASN][1000 genomes]
rs7103456	1.00[ASN][1000 genomes]
rs7113001	1.00[ASN][1000 genomes]
rs7114651	1.00[ASN][1000 genomes]
rs7116456	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7119292	1.00[ASN][1000 genomes]
rs7119383	1.00[ASN][1000 genomes]
rs7126341	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7130583	1.00[ASN][1000 genomes]
rs9804430	1.00[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	nsv897062	chr11:23687928-24031627	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv916840	chr11:23710275-24064119	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr11:23970800-23978400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr11:23973600-23975200	Weak transcription	Fetal Lung	lung

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