Table S4. The number of mutants identified through PGM sequencing.

Mutation type	Bronchiectasis patients (n=192)	Healthy subjects (n=100)
Non-synonymous SNV	277	232
synonymous SNV	138	123
Stop-gain	6	2
Frameshift insertion	1	8
Frameshift deletion	4	2
Non-frameshift variation	0	6
Unknown	21	20
Total	447	393

SNV, single nucleotide variants.