Variant report

Variant	rs2134871
Chromosome Location	chr13:61517842-61517843
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11148531	0.87[ASN][1000 genomes]
rs11840739	0.87[ASN][1000 genomes]
rs1394319	0.87[ASN][1000 genomes]
rs1410792	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1410793	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1504407	0.87[ASN][1000 genomes]
rs1504411	0.83[ASN][1000 genomes]
rs1556103	0.86[ASN][1000 genomes]
rs159885	0.85[ASN][1000 genomes]
rs1857725	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2047902	0.97[ASN][1000 genomes]
rs2047903	0.97[ASN][1000 genomes]
rs2137843	0.84[ASN][1000 genomes]
rs2137844	0.84[ASN][1000 genomes]
rs2137845	0.84[ASN][1000 genomes]
rs214120	0.85[ASN][1000 genomes]
rs2174313	0.87[ASN][1000 genomes]
rs2221400	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs301638	0.85[ASN][1000 genomes]
rs301651	0.86[ASN][1000 genomes]
rs4086378	0.83[ASN][1000 genomes]
rs7140034	0.87[ASN][1000 genomes]
rs73221633	0.89[ASN][1000 genomes]
rs7336402	0.86[ASN][1000 genomes]
rs9528260	0.85[ASN][1000 genomes]
rs9528262	0.87[ASN][1000 genomes]
rs9538970	0.86[ASN][1000 genomes]
rs9538971	0.89[ASN][1000 genomes]
rs9538973	0.85[ASN][1000 genomes]
rs9538974	0.85[ASN][1000 genomes]
rs9538975	0.84[ASN][1000 genomes]
rs9538981	0.87[ASN][1000 genomes]
rs9538984	0.97[ASN][1000 genomes]
rs9563847	0.86[ASN][1000 genomes]
rs9563848	0.87[ASN][1000 genomes]
rs9563850	0.85[ASN][1000 genomes]
rs9570388	0.86[ASN][1000 genomes]
rs9570389	0.86[ASN][1000 genomes]
rs9570391	0.85[ASN][1000 genomes]
rs9570403	0.98[ASN][1000 genomes]
rs9570404	0.98[ASN][1000 genomes]
rs9570410	0.83[ASN][1000 genomes]
rs9598189	0.87[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	chr13:61517200-61519800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr13:61517800-61519600	Weak transcription	Esophagus	oesophagus

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