Variant report

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

rs_ID	r²[population]
rs10457397	0.98[ASN][1000 genomes]
rs10499098	0.84[EUR][1000 genomes]
rs11153944	0.94[ASN][1000 genomes]
rs11961543	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11965399	0.81[EUR][1000 genomes]
rs11967874	0.84[EUR][1000 genomes]
rs11970527	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12661436	0.84[EUR][1000 genomes]
rs12663612	0.84[AFR][1000 genomes]
rs12665301	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17082730	0.84[EUR][1000 genomes]
rs17082740	0.84[EUR][1000 genomes]
rs2358048	0.90[EUR][1000 genomes]
rs4574687	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55908530	0.84[EUR][1000 genomes]
rs6933679	0.90[EUR][1000 genomes]
rs72956032	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs72968094	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72969940	0.84[EUR][1000 genomes]
rs72969948	0.81[EUR][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	esv2753290	chr6:120309301-120979301	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	esv2752474	chr6:120309301-120982301	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA	5 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	chr6:120966600-120968600	Enhancers	Fetal Lung	lung

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