Variant report

Variant	rs10963284
Chromosome Location	chr9:17811998-17811999
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10448159	0.86[CEU][hapmap]
rs10491540	0.95[CEU][hapmap];0.85[AMR][1000 genomes]
rs10810850	0.95[CEU][hapmap];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10963249	0.85[AMR][1000 genomes]
rs10963254	0.85[AMR][1000 genomes]
rs10963258	0.95[CEU][hapmap];0.85[AMR][1000 genomes]
rs10963261	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10963262	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10963263	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10963264	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10963265	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10963267	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10963268	0.95[CEU][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10963270	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10963272	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10963273	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10963274	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10963275	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10963276	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10963278	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10963288	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10963289	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1114790	0.86[CEU][hapmap]
rs12000241	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12005953	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12006023	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12006056	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12377526	1.00[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12378332	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12379450	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12380227	0.91[CEU][hapmap];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13284953	0.82[AMR][1000 genomes]
rs13290434	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13291009	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13291415	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13291891	0.82[AMR][1000 genomes]
rs1536068	0.86[CEU][hapmap]
rs2383041	0.94[CEU][hapmap]
rs34106908	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34701669	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35728688	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs36045574	0.85[AMR][1000 genomes]
rs41305339	0.87[AMR][1000 genomes]
rs4287033	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4394493	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4416918	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4487880	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4961448	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62549703	0.85[AMR][1000 genomes]
rs7044550	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7865921	0.90[CEU][hapmap]
rs9406734	0.86[CEU][hapmap]
rs9406736	0.87[CEU][hapmap]

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:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:17796000-17812000	Weak transcription	Aorta	Aorta
2	chr9:17808400-17812000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:17810600-17812600	Enhancers	Fetal Brain Male	brain
4	chr9:17810800-17812400	Enhancers	Duodenum Smooth Muscle	Duodenum
5	chr9:17811000-17812800	Enhancers	Fetal Lung	lung
6	chr9:17811200-17812400	Weak transcription	Fetal Brain Female	brain
7	chr9:17811200-17814200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr9:17811400-17812400	Enhancers	Fetal Heart	heart
9	chr9:17811400-17813000	Enhancers	Fetal Stomach	stomach
10	chr9:17811600-17812800	Enhancers	Fetal Muscle Leg	muscle
11	chr9:17811800-17812800	Enhancers	Fetal Kidney	kidney

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links