Variant report

Variant	rs26664
Chromosome Location	chr5:116171727-116171728
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10035572	0.84[ASN][1000 genomes]
rs10051070	0.86[ASN][1000 genomes]
rs10051209	0.87[ASN][1000 genomes]
rs10053269	0.85[ASN][1000 genomes]
rs10053279	0.87[ASN][1000 genomes]
rs1035861	0.87[ASN][1000 genomes]
rs10463687	0.84[ASN][1000 genomes]
rs10463688	0.84[ASN][1000 genomes]
rs11241403	0.84[ASN][1000 genomes]
rs12515978	0.94[ASN][1000 genomes]
rs13163078	0.83[ASN][1000 genomes]
rs13175939	0.83[ASN][1000 genomes]
rs1366158	0.83[ASN][1000 genomes]
rs1366159	0.83[ASN][1000 genomes]
rs153582	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs153585	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs153586	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1544742	0.84[ASN][1000 genomes]
rs253895	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs253897	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs253899	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs27514	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2900099	0.87[ASN][1000 genomes]
rs2913598	0.80[ASN][1000 genomes]
rs4920937	0.85[ASN][1000 genomes]
rs6870730	0.85[ASN][1000 genomes]
rs6896154	0.85[ASN][1000 genomes]
rs722958	0.87[ASN][1000 genomes]
rs7705356	0.84[ASN][1000 genomes]
rs7705508	0.84[ASN][1000 genomes]
rs7710040	0.84[ASN][1000 genomes]
rs7710088	0.84[ASN][1000 genomes]
rs9942388	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv527974	chr5:115987168-116303678	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv462403	chr5:115994775-116284378	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv599485	chr5:115994775-116284378	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1030056	chr5:116008971-116278725	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1033140	chr5:116035131-116314673	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1027701	chr5:116138286-116185586	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer 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	chr5:116171000-116172600	Weak transcription	HepG2	liver

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