Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12100815	0.89[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs12889947	0.90[ASN][1000 genomes]
rs12890538	0.90[ASN][1000 genomes]
rs1381621	0.96[ASN][1000 genomes]
rs1462342	0.94[ASN][1000 genomes]
rs1462343	0.95[ASN][1000 genomes]
rs1564058	0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1766150	0.82[ASN][1000 genomes]
rs1971244	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28597960	0.86[ASN][1000 genomes]
rs4899846	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4899847	0.87[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4904160	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4904161	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4904165	0.93[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs6574774	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6574775	0.89[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs7147104	0.87[ASN][1000 genomes]
rs7148162	0.94[ASN][1000 genomes]
rs7148532	0.90[ASN][1000 genomes]
rs7158569	0.90[ASN][1000 genomes]
rs7159548	0.90[ASN][1000 genomes]
rs7160548	0.83[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs9285598	0.93[ASN][1000 genomes]
rs9323742	0.93[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	nsv565376	chr14:84612088-84644822	Enhancers Weak transcription	TF binding region lncRNA	3 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	chr14:84620200-84620400	Enhancers	Fetal Heart	heart

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