Variant report

Variant	rs1792556
Chromosome Location	chr11:15244521-15244522
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10766213	0.90[JPT][hapmap]
rs10766214	0.83[ASN][1000 genomes]
rs10766215	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10766216	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10832372	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10832373	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10832374	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs10832375	0.83[ASN][1000 genomes]
rs10832376	0.83[ASN][1000 genomes]
rs11023471	0.83[ASN][1000 genomes]
rs11023472	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs11828254	0.83[ASN][1000 genomes]
rs1714333	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1714336	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1714337	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1792553	0.86[EUR][1000 genomes]
rs1792557	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs1945626	1.00[JPT][hapmap]
rs1945629	0.95[JPT][hapmap]
rs1945630	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs3110500	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs4756801	0.95[JPT][hapmap]
rs4756802	0.83[ASN][1000 genomes]
rs4757298	0.95[JPT][hapmap]
rs4757299	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs4757300	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs4757301	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs5004266	0.95[JPT][hapmap]
rs7129739	0.83[ASN][1000 genomes]
rs939048	0.88[CEU][hapmap];0.85[EUR][1000 genomes]
rs939049	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs939051	0.95[JPT][hapmap];0.81[ASN][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	nsv1038154	chr11:14991411-15246500	Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv540950	chr11:14991411-15246500	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv897007	chr11:14991411-15260124	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv530217	chr11:14991411-15275034	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2830370	chr11:15142247-15444094	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv897010	chr11:15219258-15279421	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv832072	chr11:15226843-15392190	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15222200-15244600	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr11:15231200-15246800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:15234400-15272000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr11:15242000-15269000	Weak transcription	Pancreas	Pancrea
5	chr11:15243400-15244600	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr11:15244000-15245400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:15244400-15246000	Enhancers	Pancreatic Islets	Pancreatic Islet

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