Variant report

Variant	rs4352534
Chromosome Location	chr4:55088767-55088768
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs17083988	1.00[EUR][1000 genomes]
rs17838983	1.00[EUR][1000 genomes]
rs4241981	1.00[EUR][1000 genomes]
rs58015793	1.00[EUR][1000 genomes]
rs60639295	1.00[EUR][1000 genomes]
rs61277389	1.00[EUR][1000 genomes]
rs61510049	1.00[EUR][1000 genomes]
rs6818057	1.00[EUR][1000 genomes]
rs73147749	1.00[EUR][1000 genomes]
rs73147754	1.00[EUR][1000 genomes]
rs73147760	1.00[EUR][1000 genomes]
rs73147772	1.00[EUR][1000 genomes]
rs73147780	1.00[EUR][1000 genomes]
rs73147784	1.00[EUR][1000 genomes]
rs73149516	1.00[EUR][1000 genomes]
rs73818173	1.00[EUR][1000 genomes]
rs7657528	1.00[EUR][1000 genomes]
rs7658546	1.00[EUR][1000 genomes]
rs7660482	1.00[EUR][1000 genomes]
rs7668948	1.00[EUR][1000 genomes]
rs7689472	1.00[EUR][1000 genomes]
rs7691475	1.00[EUR][1000 genomes]
rs7696276	1.00[EUR][1000 genomes]
rs7696283	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008793	chr4:55060925-55535807	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv537098	chr4:55060925-55535807	Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 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	chr4:55084200-55091200	Weak transcription	Ovary	ovary
2	chr4:55084600-55090600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:55084600-55091400	Weak transcription	Osteobl	bone
4	chr4:55084600-55092800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr4:55084800-55090600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:55084800-55091400	Weak transcription	NHLF	lung
7	chr4:55085200-55090400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:55086200-55091200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr4:55086800-55091400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links