Variant report

Variant	rs4961450
Chromosome Location	chr9:17822712-17822713
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1049430	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10756917	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10756918	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10810853	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10810854	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10963281	0.81[AMR][1000 genomes]
rs10963285	0.80[ASN][1000 genomes]
rs12552903	0.86[ASN][1000 genomes]
rs12555445	0.86[ASN][1000 genomes]
rs12555732	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13288654	0.81[ASN][1000 genomes]
rs35956180	0.85[ASN][1000 genomes]
rs4284124	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4302936	0.81[AMR][1000 genomes]
rs4373621	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4391525	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4510955	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4523358	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4599896	0.86[EUR][1000 genomes]
rs4961449	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4961451	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4961597	0.80[ASN][1000 genomes]
rs4961599	0.89[ASN][1000 genomes]
rs6475174	0.86[AMR][1000 genomes]
rs6475177	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6475178	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6475181	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7018795	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7019050	0.87[EUR][1000 genomes]
rs7023218	0.86[ASN][1000 genomes]
rs7025077	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7026318	0.86[ASN][1000 genomes]
rs7028412	0.80[AMR][1000 genomes]
rs7029727	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7039352	0.86[ASN][1000 genomes]
rs7041618	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72691895	0.86[ASN][1000 genomes]
rs7847005	0.82[ASN][1000 genomes]
rs7850617	0.86[ASN][1000 genomes]
rs7857826	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7861909	0.85[ASN][1000 genomes]
rs7863227	0.89[ASN][1000 genomes]
rs7863603	0.89[ASN][1000 genomes]
rs7863806	0.87[ASN][1000 genomes]
rs7869721	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	nsv824867	chr9:17810486-17828870	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv8422	chr9:17810758-17829560	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv2761507	chr9:17810983-17901307	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv2757321	chr9:17811584-17828437	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv2759675	chr9:17811584-17828437	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv2754695	chr9:17811600-17828400	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17817400-17823600	Weak transcription	Fetal Brain Male	brain
2	chr9:17821400-17824400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr9:17822000-17823600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:17822400-17824200	Weak transcription	Fetal Brain Female	brain

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