Variant report

Variant	rs9603186
Chromosome Location	chr13:38017181-38017182
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1107244	0.86[ASN][1000 genomes]
rs12584046	0.86[ASN][1000 genomes]
rs12584670	0.94[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs1322804	0.85[ASN][1000 genomes]
rs1570387	0.86[ASN][1000 genomes]
rs1590305	0.83[ASN][1000 genomes]
rs17055629	0.96[ASN][1000 genomes]
rs17055871	0.94[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs1853326	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1923716	0.88[ASN][1000 genomes]
rs2224659	0.85[ASN][1000 genomes]
rs2323487	0.86[ASN][1000 genomes]
rs3764077	0.86[ASN][1000 genomes]
rs3764078	0.82[ASN][1000 genomes]
rs55903929	0.84[ASN][1000 genomes]
rs56098078	0.84[ASN][1000 genomes]
rs57123822	0.82[ASN][1000 genomes]
rs58722541	0.95[ASN][1000 genomes]
rs60979745	0.82[ASN][1000 genomes]
rs61946575	0.86[ASN][1000 genomes]
rs61946576	0.86[ASN][1000 genomes]
rs61946592	0.86[ASN][1000 genomes]
rs61946593	0.86[ASN][1000 genomes]
rs61947241	0.80[ASN][1000 genomes]
rs61947266	0.95[ASN][1000 genomes]
rs61947269	0.92[ASN][1000 genomes]
rs6563537	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6563539	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6563540	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6563550	0.86[ASN][1000 genomes]
rs6563551	0.86[ASN][1000 genomes]
rs7139878	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73180681	0.86[ASN][1000 genomes]
rs7324216	0.94[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs7334573	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7334752	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7337526	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs7338422	0.95[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs7982721	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7984882	0.84[ASN][1000 genomes]
rs7986069	0.82[ASN][1000 genomes]
rs7989580	0.80[ASN][1000 genomes]
rs7994129	0.90[ASN][1000 genomes]
rs7995332	0.84[ASN][1000 genomes]
rs8001314	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs875082	0.86[ASN][1000 genomes]
rs9547852	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9547867	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9547869	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9547871	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9547873	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9547877	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9576269	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9594204	0.83[ASN][1000 genomes]
rs9594212	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9594214	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs9603182	0.80[ASN][1000 genomes]
rs9603184	0.80[ASN][1000 genomes]
rs9603185	0.99[ASN][1000 genomes]
rs9603191	0.88[ASN][1000 genomes]
rs9603194	0.90[ASN][1000 genomes]
rs9603195	0.85[ASN][1000 genomes]
rs9603210	0.91[ASN][1000 genomes]
rs9603213	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs9603214	0.85[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	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv899994	chr13:37816086-38087145	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1038850	chr13:37820489-38209571	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv34109	chr13:37843819-38276391	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv832582	chr13:37943056-38124252	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1045716	chr13:37952062-38394595	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 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	chr13:38004200-38017200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr13:38017000-38017200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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