Variant report

Variant	rs2209424
Chromosome Location	chr9:17751887-17751888
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10119271	0.95[ASN][1000 genomes]
rs10122834	0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10738488	0.94[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10738489	0.86[EUR][1000 genomes]
rs10810847	1.00[CEU][hapmap];0.85[GIH][hapmap];0.95[TSI][hapmap];0.95[EUR][1000 genomes]
rs10810851	0.96[CEU][hapmap];0.82[CHD][hapmap];0.91[TSI][hapmap];0.84[EUR][1000 genomes]
rs12377594	0.96[EUR][1000 genomes]
rs1886589	0.91[GIH][hapmap];0.93[TSI][hapmap];0.97[EUR][1000 genomes]
rs2031456	0.91[ASN][1000 genomes]
rs2182091	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[GIH][hapmap];0.88[JPT][hapmap];0.82[MEX][hapmap];0.98[TSI][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2209428	0.96[CEU][hapmap];0.84[CHB][hapmap];0.82[CHD][hapmap];0.91[TSI][hapmap];0.85[EUR][1000 genomes]
rs2209431	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2209432	0.96[CEU][hapmap];0.88[CHB][hapmap];0.88[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2224954	0.96[CEU][hapmap];0.84[CHB][hapmap];0.88[JPT][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes]
rs2224955	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2296367	0.92[CEU][hapmap];0.91[TSI][hapmap];0.91[EUR][1000 genomes]
rs2383046	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3780226	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs3808667	0.96[CEU][hapmap];0.81[GIH][hapmap];0.88[JPT][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes]
rs3808670	0.84[CHB][hapmap];0.83[JPT][hapmap];0.85[EUR][1000 genomes]
rs3808673	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs3808675	0.92[CEU][hapmap];0.91[EUR][1000 genomes]
rs3808681	1.00[CEU][hapmap];0.89[CHB][hapmap];0.82[CHD][hapmap];0.87[GIH][hapmap];0.88[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4302941	0.96[CEU][hapmap];0.82[GIH][hapmap];0.91[TSI][hapmap];0.88[EUR][1000 genomes]
rs4348595	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4961591	1.00[CHB][hapmap];0.80[CHD][hapmap];0.94[JPT][hapmap];0.95[ASN][1000 genomes]
rs7026725	0.88[ASN][1000 genomes]
rs7036431	0.84[EUR][1000 genomes]
rs7041545	0.84[CHB][hapmap];0.83[JPT][hapmap];0.86[EUR][1000 genomes]
rs9298783	0.96[CEU][hapmap];0.81[GIH][hapmap];0.88[JPT][hapmap];0.91[TSI][hapmap];0.84[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	nsv1033892	chr9:17734224-17757581	Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases
6	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
7	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

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2209424	ADAMTSL1	cis	cerebellum	SCAN
rs2209424	SH3GL2	cis	cerebellum	SCAN
rs2209424	CNTLN	cis	cerebellum	SCAN

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links