CSV tables. Rows are full-length genotypes from PacBio sequencing (Cry1ac) or 600-nt paired end Illumina sequencing (TadA). Columns are samples or timepoints. Values are frequencies such that columns
aMAF, minor allele frequency from the HapMap database for the CHB population. The difference in the genotype distributions between the case and control subjects in the co-dominant model was estimated
