Schema for EPDnew Promoters - Promoters from EPDnew
  Database: hg38    Primary Table: epdNewPromoter Data last updated: 2018-05-15
Big Bed File Download: /gbdb/hg38/bbi/epdNewHuman006.hg38.bb
Item Count: 29,598
The data is stored in the binary BigBed format.

Format description: Browser Extensible Data
fieldexampledescription
chromchr1Reference sequence chromosome or scaffold
chromStart166166977Start position in chromosome
chromEnd166167037End position in chromosome
nameFAM78B_1Name of item.
score900Score (0-1000)
strand-+ or - for strand
thickStart166166977Start of where display should be thick (start codon)
thickEnd166166988End of where display should be thick (stop codon)

Sample Rows
 
chromchromStartchromEndnamescorestrandthickStartthickEnd
chr1166166977166167037FAM78B_1900-166166977166166988
chr1166839300166839360POGK_2900+166839349166839360
chr1166839429166839489POGK_1900+166839478166839489
chr1166876246166876306TADA1_1900-166876246166876257
chr1166975356166975416ILDR2_1900-166975356166975367
chr1166975524166975584MAEL_1900+166975573166975584
chr1166989231166989291MAEL_2900+166989280166989291
chr1167090366167090426GPA33_2900-167090366167090377
chr1167090604167090664GPA33_1900-167090604167090615
chr1167094025167094085DUSP27_1900+167094074167094085

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.