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Overlap between mutations identified in MA lines/populations (SNVs) and variants detected in the 1001 Genomes population (SNPs). Comparison of expected and observed proportions of SNVs and indels that overlap the SNPs and indels in the 1001 Genomes dataset. Numbers at the tops of the bars are absolute overlap values. Asterisks indicate p < 0.05 (*), p < 0.01 (**), and p < 0.001 (***) based on Fisher’s exact test with Bonferroni correction
