Variant report

Variant	rs57266568
Chromosome Location	chr18:11407466-11407467
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs28407562	1.00[AFR][1000 genomes]
rs28773553	1.00[AFR][1000 genomes]
rs56888019	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57137930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57544896	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57710578	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58251170	1.00[AFR][1000 genomes]
rs58668675	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59908027	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59958343	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61037801	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61051889	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7226735	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7226943	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7227388	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7227901	1.00[AFR][1000 genomes]
rs7234327	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7236356	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7238464	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7238652	1.00[AMR][1000 genomes]
rs9949189	1.00[AMR][1000 genomes]
rs9950712	1.00[AMR][1000 genomes]
rs9952349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9958730	1.00[AFR][1000 genomes]
rs9961495	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9963186	1.00[AFR][1000 genomes]
rs9964299	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9966117	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv458029	chr18:10814334-11662151	Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv576480	chr18:10814334-11662151	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1066659	chr18:11246502-11709409	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
4	nsv1057976	chr18:11251898-11664914	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
5	nsv543650	chr18:11251898-11664914	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
6	nsv833589	chr18:11293101-11454521	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1056541	chr18:11336695-11558542	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv543651	chr18:11336695-11558542	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
9	nsv458031	chr18:11362587-11557161	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv576482	chr18:11362587-11557161	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11406800-11410600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr18:11407400-11408600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr18:11407400-11412400	Enhancers	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links