Variant report

Variant	rs349064
Chromosome Location	chr11:84787330-84787331
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10501585	0.92[CEU][hapmap];0.86[YRI][hapmap];0.89[AMR][1000 genomes]
rs10792795	0.83[JPT][hapmap]
rs11600088	1.00[CEU][hapmap];0.81[CHB][hapmap];0.91[YRI][hapmap]
rs11605620	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap]
rs11607636	0.85[CEU][hapmap];0.86[CHB][hapmap]
rs11607740	0.80[CHB][hapmap]
rs17207058	0.86[CEU][hapmap];0.81[CHB][hapmap];0.87[YRI][hapmap]
rs1783749	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs180954	0.92[CEU][hapmap];0.87[CHB][hapmap];0.90[YRI][hapmap];0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs349059	1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs349061	1.00[CEU][hapmap];0.81[CHB][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs349067	1.00[CEU][hapmap];0.88[CHB][hapmap];0.83[YRI][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs349074	0.81[EUR][1000 genomes]
rs349077	0.92[CEU][hapmap];0.91[JPT][hapmap];0.81[EUR][1000 genomes]
rs349079	0.92[CEU][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs349089	0.82[JPT][hapmap]
rs3907015	0.83[JPT][hapmap]
rs472375	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs472406	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs483220	0.85[CEU][hapmap];0.87[CHB][hapmap]
rs494517	0.89[AMR][1000 genomes]
rs509179	0.92[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs570423	0.89[AMR][1000 genomes]
rs573963	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs576449	0.86[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[YRI][hapmap];0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs582652	0.92[CEU][hapmap];0.87[CHB][hapmap];0.90[YRI][hapmap]
rs596423	0.92[CEU][hapmap];0.87[CHB][hapmap];0.90[YRI][hapmap];0.89[AMR][1000 genomes]
rs597604	0.86[ASN][1000 genomes]
rs612389	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs616320	0.87[JPT][hapmap]
rs623403	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs624493	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap]
rs630015	0.82[JPT][hapmap]
rs637930	0.89[AMR][1000 genomes]
rs651536	1.00[CEU][hapmap];0.81[CHB][hapmap];0.95[YRI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs659414	0.86[CEU][hapmap];0.94[CHB][hapmap];0.91[YRI][hapmap]
rs660451	0.92[CEU][hapmap];0.86[JPT][hapmap];0.83[EUR][1000 genomes]
rs660860	1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap]
rs664417	0.92[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs678796	0.81[CHB][hapmap];0.91[YRI][hapmap];0.80[AMR][1000 genomes]
rs7931733	0.91[JPT][hapmap]

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	nsv948410	chr11:83918339-84812001	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv430415	chr11:84661652-84833852	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1055097	chr11:84672444-84810441	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1040393	chr11:84708402-84866594	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv527535	chr11:84724795-84895033	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv528491	chr11:84724795-84895033	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84783800-84787400	Weak transcription	Left Ventricle	heart
2	chr11:84787000-84788200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr11:84787000-84789000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:84787200-84788000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr11:84787200-84788000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:84787200-84788200	Enhancers	NH-A	brain
7	chr11:84787200-84788400	Enhancers	Fetal Heart	heart
8	chr11:84787200-84788600	Enhancers	NHDF-Ad	bronchial
9	chr11:84787200-84789400	Enhancers	NHEK	skin

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