For three pediatric tumor types, we identified aberrant methylation events (either hypomethylation or hypermethylation) that had occurred in a given tumor and gene. For the same tumor/gene combinations, we identified somatic single-nucleotide variants, indels, and structural variants that had occurred. These numbers indicate overall rates of aberrant methylation or mutation across all tumors of a given type. Methylation rates and mutation rates were typically similar across all three gene categories, but mutation rates for oncogenes and tumor suppressor genes were always higher than for other genes.