Variant report

Variant	rs12153556
Chromosome Location	chr5:52735868-52735869
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1030227	0.91[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10940312	0.86[ASN][1000 genomes]
rs11740573	0.87[ASN][1000 genomes]
rs11741921	0.84[ASN][1000 genomes]
rs11742633	0.94[ASN][1000 genomes]
rs11745102	0.94[ASN][1000 genomes]
rs11748901	0.94[ASN][1000 genomes]
rs12153178	0.87[ASN][1000 genomes]
rs12153379	0.82[ASN][1000 genomes]
rs13153643	0.94[ASN][1000 genomes]
rs13157909	0.87[ASN][1000 genomes]
rs13161996	0.87[ASN][1000 genomes]
rs13162472	0.90[ASN][1000 genomes]
rs13163361	0.90[ASN][1000 genomes]
rs13170709	0.95[ASN][1000 genomes]
rs13176460	0.90[ASN][1000 genomes]
rs13179666	0.86[ASN][1000 genomes]
rs13188772	0.94[ASN][1000 genomes]
rs1363971	0.81[ASN][1000 genomes]
rs1423549	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1423559	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1423561	0.82[ASN][1000 genomes]
rs1469100	0.82[ASN][1000 genomes]
rs2042331	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34274925	0.90[ASN][1000 genomes]
rs34483113	0.94[ASN][1000 genomes]
rs34492969	0.90[ASN][1000 genomes]
rs34547502	0.81[ASN][1000 genomes]
rs34690366	0.86[ASN][1000 genomes]
rs34762534	0.93[ASN][1000 genomes]
rs34985749	0.80[ASN][1000 genomes]
rs35257227	0.94[ASN][1000 genomes]
rs36125518	0.86[ASN][1000 genomes]
rs3943929	0.82[ASN][1000 genomes]
rs4254863	0.94[ASN][1000 genomes]
rs4279297	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs71592629	0.94[ASN][1000 genomes]
rs71619953	0.90[ASN][1000 genomes]
rs9686990	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949005	chr5:52188028-52808229	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2752745	chr5:52422063-53343529	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1032632	chr5:52667145-53655624	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 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	chr5:52734000-52736400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:52734200-52736000	Enhancers	NHDF-Ad	bronchial
3	chr5:52734200-52736200	Enhancers	Colon Smooth Muscle	Colon
4	chr5:52734200-52736800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:52735000-52736000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:52735000-52736000	Weak transcription	NHLF	lung
7	chr5:52735000-52736200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:52735800-52736600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr5:52735800-52738400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links