Additional file 1 of Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences

Additional file 1: Table S1A. Detected CFTR variants across UKBB populations. Table S1B. CFTR2 CF-causing variants excluded/included in our analysis. Table S2. Unique CF-causing variants. Table S3. CF-causing CFTR variants. Table S4. Variable clinical consequence variants detected across UKBB ancestries. Table S5. Unique CF-causing variants. Table S6. Common varying clinical consequences (VCC) variants. Table S7. CFTR variants annotated as having High Impact. Table S8. Uncharacterized high impact variants. Table S9. High impact and CF-Causing variants. Table S10. Dated variants within the CFTR gene locus.