Variant report

Variant	rs294018
Chromosome Location	chr11:26532286-26532287
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 111 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:105)

rs_ID	r²[population]
rs10501051	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs10501053	0.83[CHD][hapmap]
rs10501056	0.86[EUR][1000 genomes]
rs10742142	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs10742143	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs10742144	0.85[CHB][hapmap];0.91[JPT][hapmap]
rs10742145	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs10767542	0.86[EUR][1000 genomes]
rs10767544	1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10767545	0.92[JPT][hapmap];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10767546	0.82[ASN][1000 genomes]
rs10767552	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs10767553	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs10834986	0.81[TSI][hapmap]
rs10834996	0.82[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10834997	0.82[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10834999	0.91[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11029576	0.82[TSI][hapmap]
rs11029577	0.82[TSI][hapmap]
rs11029582	0.87[CHD][hapmap]
rs11029583	0.87[CHD][hapmap]
rs11029595	1.00[CHB][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs11029596	0.83[ASN][1000 genomes]
rs11029598	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs11029600	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs1125621	0.81[TSI][hapmap]
rs11823219	0.86[CHB][hapmap];0.87[CHD][hapmap];0.92[JPT][hapmap]
rs11825007	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs1389459	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1472933	0.81[ASN][1000 genomes]
rs1493742	0.96[CHD][hapmap];0.92[JPT][hapmap]
rs16915828	1.00[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs1848562	0.85[EUR][1000 genomes]
rs1960088	0.84[EUR][1000 genomes]
rs2087972	0.85[EUR][1000 genomes]
rs2087974	0.85[JPT][hapmap]
rs2663165	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs2663168	0.82[CEU][hapmap];0.96[CHD][hapmap];0.92[JPT][hapmap]
rs2663170	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs2663171	0.81[CEU][hapmap];0.92[JPT][hapmap]
rs2703403	0.82[CEU][hapmap];0.90[CHD][hapmap];0.92[JPT][hapmap]
rs2703404	0.87[CHD][hapmap];0.92[JPT][hapmap]
rs2703408	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs2703411	0.92[JPT][hapmap]
rs2703413	0.89[JPT][hapmap]
rs2703417	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2703418	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs2703422	0.86[CHB][hapmap];0.87[CHD][hapmap];0.92[JPT][hapmap]
rs2860040	0.82[TSI][hapmap]
rs293939	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs293940	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs293941	0.86[CHB][hapmap];0.87[CHD][hapmap];0.92[JPT][hapmap]
rs293943	0.86[CHB][hapmap];0.87[CHD][hapmap];0.92[JPT][hapmap]
rs294011	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs294012	0.85[ASW][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap];0.97[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs294013	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs294014	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs294015	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs294020	0.91[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs294021	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs294027	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[MKK][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs294028	0.91[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3105881	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs3105884	0.82[CEU][hapmap];0.96[CHD][hapmap];0.92[JPT][hapmap]
rs364850	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs365243	0.82[CEU][hapmap];0.92[JPT][hapmap]
rs367624	0.82[CEU][hapmap];0.92[JPT][hapmap]
rs368786	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs372878	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs375773	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs383137	1.00[CHB][hapmap];0.92[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs383158	0.85[CHB][hapmap];0.92[JPT][hapmap]
rs389022	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs389051	0.85[ASW][hapmap];0.86[CHB][hapmap];0.87[CHD][hapmap];0.82[GIH][hapmap];0.92[JPT][hapmap];0.97[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs392240	0.86[CHB][hapmap];0.91[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs396607	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap]
rs397696	0.92[JPT][hapmap]
rs398191	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs398314	0.86[CHB][hapmap];0.87[CHD][hapmap];0.92[JPT][hapmap]
rs4032916	0.84[EUR][1000 genomes]
rs407632	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs410036	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs410617	0.93[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs415964	0.85[CHB][hapmap];0.91[JPT][hapmap]
rs420143	0.87[CHD][hapmap]
rs425806	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs427800	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs430563	0.92[ASW][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.90[GIH][hapmap];0.83[JPT][hapmap];0.97[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs431479	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs439065	0.86[CHB][hapmap];0.82[CHD][hapmap];0.91[JPT][hapmap]
rs440645	0.82[CEU][hapmap];0.96[CHD][hapmap];0.92[JPT][hapmap]
rs4444033	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs444534	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs444622	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs4923362	0.92[JPT][hapmap]
rs4923364	0.92[JPT][hapmap]
rs511371	0.85[CHB][hapmap];0.91[JPT][hapmap]
rs550083	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs551759	0.86[CHB][hapmap];0.92[JPT][hapmap]
rs7119396	0.91[CEU][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7126899	0.90[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs721258	0.85[JPT][hapmap]
rs72891214	0.93[ASN][1000 genomes]
rs7945815	0.91[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9988806	0.86[CHB][hapmap];0.92[JPT][hapmap]

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	nsv1051211	chr11:26473131-26604553	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv467778	chr11:26485520-26603926	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv553899	chr11:26485520-26603926	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv521916	chr11:26485520-26605331	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1044544	chr11:26506962-26967285	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv1039308	chr11:26529848-26555414	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	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	chr11:26506400-26564600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr11:26531200-26533800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:26532000-26532600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr11:26532000-26532600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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