Variant report

Variant	rs9406698
Chromosome Location	chr9:17765336-17765337
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11791520	0.81[EUR][1000 genomes]
rs2182082	0.87[EUR][1000 genomes]
rs2209426	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2209427	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2209429	0.87[EUR][1000 genomes]
rs2224953	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2274216	0.92[EUR][1000 genomes]
rs4141716	0.81[EUR][1000 genomes]
rs4961595	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6475171	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6475172	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7020594	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7032090	0.87[EUR][1000 genomes]
rs7851224	0.93[EUR][1000 genomes]
rs7858932	0.92[EUR][1000 genomes]
rs7868359	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9407845	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9407846	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892675	chr9:17694823-17790526	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv613706	chr9:17718918-18090934	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv613707	chr9:17720175-18070475	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv613708	chr9:17720175-18072085	Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1034673	chr9:17739006-17916606	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1023089	chr9:17748811-17919574	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv16404	chr9:17764515-17765573	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17754800-17772600	Weak transcription	Hela-S3	cervix
2	chr9:17764600-17782800	Weak transcription	Gastric	stomach
3	chr9:17765200-17766200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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