Additional file 1 of Whole genome sequencing reveals the independent clonal origin of multifocal ileal neuroendocrine tumors

Additional file 1: Table S1. WGS sample information and somatic genomic alteration counts. Table S3. Filtered copy-number alteration calls. Table S4. Filtered structural variant calls. Table S5. MutSig2CV results for patient-level information. Table S6. MutSig2CV results for tumor-level information. Table S7. Recurrent non-coding variants. Table S8. Results of the signaling pathway analysis. Table S9. Results of chromosome mapping analysis