The somatic base substitutions in the whole genome sequenced single skin cell clonal lineages.

a) The fraction of all SNVs prior to filtering that correspond to each allele frequency bin. SNVs that corresponded to allele frequencies between 45% and 55% or above 90% were considered clonal. b) The exonic somatic base substitutions in the samples. c) The mutation spectra in the samples. The reverse complements are considered in the mutation spectra analyses. (XLSX)