Variant report

Variant	rs8000641
Chromosome Location	chr13:110582921-110582922
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs1333982	0.90[EUR][1000 genomes]
rs1333984	0.82[ASN][1000 genomes]
rs1333987	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1556571	0.83[ASN][1000 genomes]
rs1556572	0.83[ASN][1000 genomes]
rs1556573	0.82[ASN][1000 genomes]
rs1855439	0.83[ASN][1000 genomes]
rs186764	0.82[ASN][1000 genomes]
rs372641	0.82[ASN][1000 genomes]
rs375176	0.82[ASN][1000 genomes]
rs422209	0.82[ASN][1000 genomes]
rs452964	0.82[ASN][1000 genomes]
rs56296105	0.88[EUR][1000 genomes]
rs58503998	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72652006	0.88[EUR][1000 genomes]
rs72652007	0.87[EUR][1000 genomes]
rs72652014	0.87[EUR][1000 genomes]
rs72670106	0.82[ASN][1000 genomes]
rs72670114	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72670117	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72670118	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72670125	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72670128	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72670134	0.91[EUR][1000 genomes]
rs72670135	0.91[EUR][1000 genomes]
rs72670137	0.88[EUR][1000 genomes]
rs7330996	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7332564	0.87[EUR][1000 genomes]
rs7999512	0.87[EUR][1000 genomes]
rs8000582	0.82[ASN][1000 genomes]
rs915017	0.85[EUR][1000 genomes]
rs915018	0.90[EUR][1000 genomes]
rs9555649	0.83[ASN][1000 genomes]
rs9555650	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9555651	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9555653	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9555654	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9555658	0.88[EUR][1000 genomes]
rs9555659	0.87[EUR][1000 genomes]
rs9555660	0.88[EUR][1000 genomes]
rs9559672	0.83[ASN][1000 genomes]
rs9559673	0.83[ASN][1000 genomes]
rs9559676	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9559677	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9559679	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9559681	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9559688	0.91[EUR][1000 genomes]
rs9559691	0.91[EUR][1000 genomes]
rs9559693	0.88[EUR][1000 genomes]
rs9559694	0.88[EUR][1000 genomes]
rs9559695	0.88[EUR][1000 genomes]
rs9559696	0.88[EUR][1000 genomes]
rs9559697	0.88[EUR][1000 genomes]
rs9559698	0.88[EUR][1000 genomes]
rs9559700	0.88[EUR][1000 genomes]
rs9559701	0.88[EUR][1000 genomes]
rs9559705	0.87[EUR][1000 genomes]
rs9559706	0.87[EUR][1000 genomes]
rs9559707	0.87[EUR][1000 genomes]
rs9583442	0.82[AFR][1000 genomes]
rs9588040	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9634587	0.82[ASN][1000 genomes]
rs9634589	0.82[ASN][1000 genomes]
rs9634590	0.82[ASN][1000 genomes]
rs9989064	0.90[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	nsv832719	chr13:110512259-110655883	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110566800-110590400	Weak transcription	Aorta	Aorta
2	chr13:110571000-110586000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:110579800-110584400	Weak transcription	Muscle Satellite Cultured Cells	--

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