Dataset for: Tobacco exposure and somatic mutations in normal human bronchial epithelium

These are mutation calls to support the paper 'Tobacco exposure and somatic mutations in normal human bronchial epithelium', which has the following authors and affiliations: Authors: Kenichi Yoshida (1) *; Kate HC Gowers (2) *; Henry Lee-Six (1); Deepak P Chandrasekharan (2); Tim Coorens (1); Elizabeth F Maughan (2); Kathryn Beal (1); Andrew Menzies (1); Fraser R Millar (2); Elizabeth Anderson (1); Sarah E Clarke (2); Adam Pennycuick (2); Ricky M Thakrar (2,3); Colin R Butler (2,3); Nobuyuki Kakiuchi (4); Tomonori Hirano (4); Robert E Hynds (2,5); Michael R Stratton (1); Inigo Martincorena (1); Sam M Janes (2,3) §; Peter J Campbell (1,6) §. * These authors contributed equally to the manuscript § Joint corresponding authors Institutes: (1) Cancer Genome Project, Wellcome Trust Sanger Institute, Hinxton, CB10 1SA, UK (2) Lungs For Living Research Centre, UCL Respiratory, University College London, London, WC1E 6JF, UK (3) Department of Thoracic Medicine, University College London Hospital, London, UK (4) Department of Pathology and Tumor Biology, Kyoto University, Kyoto, Japan (5) CRUK Lung Cancer Centre of Excellence, UCL Cancer Institute, University College London, London, UK (6) Stem Cell Institute, University of Cambridge, Hills Rd, Cambridge, UK The data are somatically acquired single base substitutions (subs), indels and structural variants called in 632 single cell-derived colonies from normal basal bronchial epithelium, across 16 subjects. The columns in the tables are interpreted as follows: Sample: ID for the colony that was whole-genome sequenced, Chrom: Chromosome the mutation was located on, Pos: Genomic position on the chromosome for the mutation (genome build GRCh37d5), Ref: The reference base at that position, Alt: The alternate allele created by the mutation, DEP: The total read depth at that position, MTR: The number of reads reporting the mutant (Alt) allele at that position in that cell, VAF: Variant allele fraction of the mutation.