Variant report

Variant	rs7206696
Chromosome Location	chr16:59606504-59606505
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10083796	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10492918	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12597033	0.87[EUR][1000 genomes]
rs12709032	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1500294	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1500295	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1500297	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1566438	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1818069	0.81[EUR][1000 genomes]
rs1818071	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1827203	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2202009	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2202010	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2202011	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2221183	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28841687	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4633709	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6500043	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6500047	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7191971	0.80[EUR][1000 genomes]
rs7192390	0.80[EUR][1000 genomes]
rs7198362	0.94[EUR][1000 genomes]
rs8046365	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8052045	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8054889	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8056444	0.81[EUR][1000 genomes]
rs8063284	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8063752	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs882854	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9302715	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9302716	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9921279	0.90[EUR][1000 genomes]
rs9922699	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9929021	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9933491	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9934111	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9937266	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9939480	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9940831	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv906747	chr16:59385832-60172030	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv916423	chr16:59411801-59750824	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv572832	chr16:59578561-59756567	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr16:59606400-59606800	ZNF genes & repeats	A549	lung

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