Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11766249	1.00[ASN][1000 genomes]
rs11769918	1.00[ASN][1000 genomes]
rs12530505	1.00[ASN][1000 genomes]
rs12536432	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12539308	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13228582	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13232332	1.00[ASN][1000 genomes]
rs13236030	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404409	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17147221	1.00[ASN][1000 genomes]
rs17472207	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1917364	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2107931	1.00[ASN][1000 genomes]
rs2402738	1.00[ASN][1000 genomes]
rs34000854	1.00[ASN][1000 genomes]
rs34799484	1.00[ASN][1000 genomes]
rs35966180	1.00[ASN][1000 genomes]
rs36008540	1.00[ASN][1000 genomes]
rs4532546	1.00[ASN][1000 genomes]
rs4731184	1.00[ASN][1000 genomes]
rs4731185	1.00[ASN][1000 genomes]
rs57462590	1.00[ASN][1000 genomes]
rs66469910	1.00[ASN][1000 genomes]
rs6962872	1.00[ASN][1000 genomes]
rs71576208	1.00[ASN][1000 genomes]
rs717240	1.00[ASN][1000 genomes]
rs9768851	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	nsv429809	chr7:123937674-124835925	Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
2	nsv831118	chr7:124172267-124347527	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:124207200-124208800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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