Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10228492	0.91[EUR][1000 genomes]
rs10239380	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10950516	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10950517	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10950518	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2108514	0.90[EUR][1000 genomes]
rs2108515	0.90[EUR][1000 genomes]
rs2159020	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2215037	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4404823	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4463321	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4719398	0.80[EUR][1000 genomes]
rs4721319	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6415237	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6461083	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6962476	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7785249	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7793052	0.91[EUR][1000 genomes]
rs7796825	0.92[EUR][1000 genomes]
rs979720	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr7:14325600-14327200	Weak transcription	Fetal Heart	heart

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