Variant report

Variant	rs9791001
Chromosome Location	chr5:92508851-92508852
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10428523	0.99[ASN][1000 genomes]
rs11738974	0.99[ASN][1000 genomes]
rs11742251	0.97[ASN][1000 genomes]
rs11743310	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12054781	0.89[ASN][1000 genomes]
rs34700540	0.96[ASN][1000 genomes]
rs4242240	1.00[ASN][1000 genomes]
rs4242241	1.00[ASN][1000 genomes]
rs4242242	0.99[ASN][1000 genomes]
rs4242244	0.82[ASN][1000 genomes]
rs4264926	1.00[ASN][1000 genomes]
rs4266388	0.95[ASN][1000 genomes]
rs4285204	1.00[ASN][1000 genomes]
rs4293897	0.96[ASN][1000 genomes]
rs4302568	1.00[ASN][1000 genomes]
rs4321736	0.99[ASN][1000 genomes]
rs4370258	0.87[ASN][1000 genomes]
rs4449514	1.00[ASN][1000 genomes]
rs4469186	1.00[ASN][1000 genomes]
rs4551050	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4551051	1.00[ASN][1000 genomes]
rs4554194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4557386	0.99[ASN][1000 genomes]
rs4632783	1.00[ASN][1000 genomes]
rs4869191	1.00[ASN][1000 genomes]
rs4869415	1.00[ASN][1000 genomes]
rs4869417	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55993462	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57542119	0.99[ASN][1000 genomes]
rs59262698	0.99[ASN][1000 genomes]
rs6557066	0.96[ASN][1000 genomes]
rs66467168	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs66624622	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67069214	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67217436	1.00[ASN][1000 genomes]
rs67735054	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67862943	0.99[ASN][1000 genomes]
rs6863269	0.97[ASN][1000 genomes]
rs6873367	0.82[ASN][1000 genomes]
rs6897863	0.98[ASN][1000 genomes]
rs7700810	0.99[ASN][1000 genomes]
rs7714485	0.99[ASN][1000 genomes]
rs7715730	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7722144	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7722718	0.99[ASN][1000 genomes]
rs9764490	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9790989	0.98[AMR][1000 genomes];0.93[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	nsv1029175	chr5:92436038-92548473	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:92500800-92521600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:92508600-92509000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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