Variant report

Variant	rs293982
Chromosome Location	chr11:26601395-26601396
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10501057	1.00[CHB][hapmap]
rs11029601	1.00[CHB][hapmap]
rs11029604	1.00[CHB][hapmap]
rs11029605	1.00[CHB][hapmap]
rs11029609	1.00[CHB][hapmap]
rs11029610	1.00[CHB][hapmap]
rs11029611	1.00[CHB][hapmap]
rs11029615	1.00[CHB][hapmap]
rs12271337	1.00[CHB][hapmap]
rs12279543	1.00[CHB][hapmap]
rs12282977	1.00[CHB][hapmap]
rs1690067	1.00[CHB][hapmap]
rs172415	1.00[CHB][hapmap]
rs188389	1.00[CHB][hapmap]
rs293955	1.00[CHB][hapmap]
rs293970	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[YRI][hapmap];0.97[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs293971	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs293985	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs293986	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs293998	1.00[CHB][hapmap]
rs380170	1.00[CHB][hapmap]
rs381229	1.00[CHB][hapmap]
rs415390	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs446946	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs724203	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 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	nsv1050121	chr11:26532655-26675303	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv540974	chr11:26532655-26675303	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv916187	chr11:26576875-27328603	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26599800-26601600	Enhancers	NHEK	skin
2	chr11:26600000-26601600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:26600000-26601600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr11:26600000-26601800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:26600200-26601400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr11:26600200-26601600	Enhancers	HMEC	breast
7	chr11:26600200-26602800	Enhancers	Fetal Lung	lung
8	chr11:26600200-26603600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr11:26600400-26602800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:26600400-26643000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr11:26600600-26601400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr11:26600600-26601600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:26600800-26601400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr11:26600800-26601400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr11:26600800-26601600	Enhancers	NHDF-Ad	bronchial
16	chr11:26600800-26602800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr11:26601000-26601600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr11:26601000-26602000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:26601000-26602600	Weak transcription	A549	lung
20	chr11:26601200-26601600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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