Schema for EPDnew Promoters - Promoters from EPDnew
  Database: mm10    Primary Table: epdNewPromoterNonCoding Data last updated: 2019-08-27
Big Bed File Download: /gbdb/mm10/bbi/epdNewMouseNc001.mm10.bb
Item Count: 3,077
The data is stored in the binary BigBed format.

Format description: Browser Extensible Data
fieldexampledescription
chromchr1Reference sequence chromosome or scaffold
chromStart130462527Start position in chromosome
chromEnd130462587End position in chromosome
nameGm16083_1Name of item.
score900Score (0-1000)
strand++ or - for strand
thickStart130462576Start of where display should be thick (start codon)
thickEnd130462587End of where display should be thick (stop codon)

Sample Rows
 
chromchromStartchromEndnamescorestrandthickStartthickEnd
chr1130462527130462587Gm16083_1900+130462576130462587
chr1130741280130741340Gm28857_1900-130741280130741291
chr1130820713130820773Gm15848_1900-130820713130820724
chr1131962944131963004Gm29103_1900+131962993131963004
chr1132342013132342073F730311O21Rik_1900+132342062132342073
chr11324770451324771056030442K20Rik_1900-132477045132477056
chr1132729319132729379Gm10538_1900+132729368132729379
chr1133068385133068445Gm28609_1900-133068385133068396
chr1133610362133610422Gm26706_1900+133610411133610422
chr1134435586134435646Platr1_1900+134435635134435646

EPDnew Promoters (epdNew) Track Description
 

Description

These tracks represent the experimentally validated promoters generated by the Eukaryotic Promoter Database.

Display Conventions and Configuration

Each item in the track is a representation of the promoter sequence identified by EPD. The "thin" part of the element represents the 49 bp upstream of the annotated transcription start site (TSS) whereas the "thick" part represents the TSS plus 10 bp downstream. The relative position of the thick and thin parts define the orientation of the promoter.

Note that the EPD team has created a public track hub containing promoter and supporting annotations for human, mouse, and other vertebrate and model organism genomes.

Methods

Briefly, gene transcript coordinates were obtained from multiple sources (HGNC, GENCODE, Ensembl, RefSeq) and validated using data from CAGE and RAMPAGE experimental studies obtained from FANTOM 5, UCSC, and ENCODE. Peak calling, clustering and filtering based on relative expression were applied to identify the most expressed promoters and those present in the largest number of samples.

For the methodology and principles used by EPD to predict TSSs, refer to Dreos et al. (2013) in the References section below. A more detailed description of how this data was generated can be found at the following links:

Credits

Data was generated by the EPD team at the Swiss Institute of Bioinformatics. For inquiries, contact the EPD team using this on-line form or email philipp. bucher@epfl. ch .

References

Dreos R, Ambrosini G, Perier RC, Bucher P. EPD and EPDnew, high-quality promoter resources in the next-generation sequencing era. Nucleic Acids Res. 2013 Jan 1;41(D1):D157-64. PMID: 23193273.