Schema for EPDnew Promoters - Promoters from EPDnew
  Database: hg38    Primary Table: epdNewPromoterNonCoding Data last updated: 2019-04-17
Big Bed File Download: /gbdb/hg38/bbi/epdNewHumanNc001.hg38.bb
Item Count: 2,339
The data is stored in the binary BigBed format.

Format description: Browser Extensible Data
fieldexampledescription
chromchr1Reference sequence chromosome or scaffold
chromStart166490012Start position in chromosome
chromEnd166490072End position in chromosome
nameLINC01675_1Name of item.
score900Score (0-1000)
strand-+ or - for strand
thickStart166490012Start of where display should be thick (start codon)
thickEnd166490023End of where display should be thick (stop codon)

Sample Rows
 
chromchromStartchromEndnamescorestrandthickStartthickEnd
chr1166490012166490072LINC01675_1900-166490012166490023
chr1168786872168786932LINC00626_1900+168786921168786932
chr1169087040169087100LINC00970_1900-169087040169087051
chr1170532031170532091GORAB-AS1_1900-170532031170532042
chr1172142615172142675DNM3OS_2900-172142615172142626
chr1172144783172144843DNM3OS_1900-172144783172144794
chr1173863206173863266GAS5-AS1_1900+173863255173863266
chr1177351530177351590LINC01645_1900+177351579177351590
chr1178093616178093676RASAL2-AS1_2900-178093616178093627
chr1178093999178094059RASAL2-AS1_1900-178093999178094010

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.