Variant report

Variant	rs4426644
Chromosome Location	chr3:25181563-25181564
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11129183	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11129184	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11129186	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11129187	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12495790	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13077701	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13098413	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1580814	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1587422	0.80[EUR][1000 genomes]
rs1587423	0.80[EUR][1000 genomes]
rs35550696	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4300979	0.86[ASN][1000 genomes]
rs4393870	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4542987	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4583609	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4586772	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4858709	0.82[ASN][1000 genomes]
rs6764917	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6804502	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs71622798	0.86[EUR][1000 genomes]
rs7616818	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7640943	0.84[ASN][1000 genomes]
rs7643390	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7643392	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7653318	0.87[ASN][1000 genomes]
rs7653321	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9861111	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9871379	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9877845	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs997309	0.82[EUR][1000 genomes];0.89[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	nsv1013446	chr3:25176609-25221334	Weak transcription Enhancers 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	chr3:25175800-25184200	Weak transcription	Fetal Lung	lung

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