Vierstra, J. et al. Global reference mapping of human transcription factor footprints. Nature 583, 729–736 (2020). https://doi.org/10.1038/s41586-020-2528-x Preprint @ bioRxiv: https://doi.org/10.1101/2020.01.31.927798 Contact: Jeff Vierstra (jvierstra@altius.org) Genomic DNase I footprinting enables quantitative, nucleotide-resolution delineation of sites of transcription factor occupancy within native chromatin. We combined sampling of >67 billion uniquely mapping DNase I cleavages from >240 human cell types and states to index, with unprecedented accuracy and resolution, human genomic footprints and thereby the sequence elements that encode transcription factor recognition sites. Please see http://vierstra.org/resources/dgf for additional information and a complete set of raw DNase I data for individual datasets. Additionally, raw data can also be accessed via the ENCODE data portal (http://encodeproject.org) using the dataset accessions found in Supplementary Table 1. Code for footprint analysis and tutorials on how to access and manipulate digital genomic footprint data can be found at https://footprint-tools.readthedocs.io/en/latest/. All files herein correspond to human genome build version GRCh38 (UCSC hg38). Dataset contents: Biosample metadata – Supplementary_Table_1.xlsx Motif clustering metadata – Supplementary_Table_2.xlsx ChIP-seq validation metadata – Supplementary_Table_3.xlsx Consensus footprint coordinates and assigned motif archetypes TSV file (BED-format) with consensus footprint (posterior probability>0.99) coordinates and overlaps with matches to motif model clusters. The legend file contains column definitions in detail. consensus_footprints_and_motifs_hg38.bed.gz consensus_footprints_and_motifs_legend.txt Motif archetype matches overlapping consensus footprints TSV file (BED-format) containing the coordinates for clustered motif model matches that overlap consensus footprints collapsed_motifs_overlaping_consensus_footprints.bed.gz collapsed_motifs_overlaping_consensus_footprints_legend.txt Footprint occupancy matrix of consensus footprints Rows are same order as the consensus footprint file and columns are same order as in the metadata files. consensus_index_matrix_full_hg38.txt.gz (Values are –log(1-posterior)) consensus_index_matrix_binary_hg38.txt.gz (binary occupancy matrix, where footprints with posterior footprint probability >0.99 are considered occupied) Single nucleotide variants tested for allelic imbalance The legend file contains column definitions in detail. genotypes.vcf.gz - Genotyping and allelic read depth for each biosample (see header for more information) tested_snvs_padj.bed.gz - SNVs tested for imbalance (TSV, BED-format) tested_snvs_padj_legend.txt

{"references": ["Vierstra et al. Global reference mapping and dynamics of human transcription factor footprints. (2020). bioRxiv"]}

This work was supported by NIH grants U54HG007010 and 5UM1HG009444.