Variant report

Variant	rs9967293
Chromosome Location	chr18:28877283-28877284
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 104 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs10163619	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10164077	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10438909	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10438930	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11081690	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11081691	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1154850	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1154851	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11660608	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11660638	1.00[ASN][1000 genomes]
rs11661048	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11661104	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11663622	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11663676	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11663924	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11872734	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11873223	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11873281	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11875510	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11875560	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11876962	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12607370	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12962355	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12963302	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12967407	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1426310	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1426311	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1460599	0.85[ASN][1000 genomes]
rs17658464	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1834582	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1895902	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2007149	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2114269	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2162273	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2199301	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2219582	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2219583	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2901124	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2901125	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs34248946	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs35136508	1.00[ASN][1000 genomes]
rs35223713	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35257361	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs35287825	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35382145	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4356544	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55778425	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs55965644	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56088904	0.82[EUR][1000 genomes]
rs62088665	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62088675	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62090169	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6506910	0.82[EUR][1000 genomes]
rs6506912	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6506915	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6506916	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67550130	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7227412	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7229763	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7229799	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7230092	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7231346	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7231775	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7234662	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7234854	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7235354	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7235951	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7235975	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7236225	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7236309	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7236370	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7237370	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7237383	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7237419	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7241874	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7244719	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7245063	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs765054	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8087410	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8087621	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8088418	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8091151	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs8091579	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8091847	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8091934	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8092044	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9944661	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9947296	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9947444	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9950209	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9950622	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9951341	1.00[ASN][1000 genomes]
rs9953981	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9954315	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9955239	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9955289	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9956026	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9959406	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9962740	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9966267	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3360998	chr18:28693111-28881812	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1066692	chr18:28856066-29190505	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv543674	chr18:28856066-29190505	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	esv3422577	chr18:28862003-28881811	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28874600-28880400	Weak transcription	Stomach Mucosa	stomach
2	chr18:28876600-28877600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr18:28876800-28877600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr18:28876800-28877800	Enhancers	NHEK	skin
5	chr18:28877000-28877600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr18:28877000-28883600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr18:28877200-28877600	Enhancers	HMEC	breast

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