Selection of annotated tumor-specific variants found in common between FF and FFPE colon samples.

Chr: chromosome number. Position: position of the variant on the chromosome. Ns: number of samples in which the variant was found. COSMIC ID: COSMIC database identification code. Gene Symbol: HGNC gene symbol. Pathways: selection of KEGG or REACTOME pathways in which the gene is involved. FFV: mean variant allelic frequency (%) for FF samples. FFD: mean read depth for the position for FF samples (coverage). FEV: mean variant allelic frequency (%) for FFPE samples. FED: mean read depth for the position for FFPE samples (coverage).