Variant report

Variant	rs2047902
Chromosome Location	chr13:61505977-61505978
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11148531	0.90[ASN][1000 genomes]
rs11840739	0.90[ASN][1000 genomes]
rs1394319	0.90[ASN][1000 genomes]
rs1410792	0.98[ASN][1000 genomes]
rs1410793	0.97[ASN][1000 genomes]
rs1504407	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1504411	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1556103	0.89[ASN][1000 genomes]
rs159885	0.89[ASN][1000 genomes]
rs1857725	0.98[ASN][1000 genomes]
rs1983090	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2047903	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2134871	0.97[ASN][1000 genomes]
rs2137843	0.87[ASN][1000 genomes]
rs2137844	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2137845	0.87[ASN][1000 genomes]
rs214120	0.89[ASN][1000 genomes]
rs2174313	0.90[ASN][1000 genomes]
rs2221400	0.95[ASN][1000 genomes]
rs301638	0.89[ASN][1000 genomes]
rs301651	0.89[ASN][1000 genomes]
rs4086378	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7140034	0.90[ASN][1000 genomes]
rs73221633	0.89[ASN][1000 genomes]
rs7336402	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9528260	0.89[ASN][1000 genomes]
rs9528262	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9538970	0.89[ASN][1000 genomes]
rs9538971	0.89[ASN][1000 genomes]
rs9538973	0.89[ASN][1000 genomes]
rs9538974	0.89[ASN][1000 genomes]
rs9538975	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9538981	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9538984	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9563847	0.89[ASN][1000 genomes]
rs9563848	0.90[ASN][1000 genomes]
rs9563850	0.89[ASN][1000 genomes]
rs9570388	0.89[ASN][1000 genomes]
rs9570389	0.89[ASN][1000 genomes]
rs9570391	0.89[ASN][1000 genomes]
rs9570403	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9570404	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9570410	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9598189	0.90[ASN][1000 genomes]
rs9598204	0.98[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	nsv832624	chr13:61383648-61553974	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61505000-61508400	Enhancers	NHEK	skin
2	chr13:61505200-61508200	Enhancers	HUVEC	blood vessel

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