Missing coverage evidence...
			seq id	start	end	size	←reads	reads→	gene	description
*	*	÷	NC_002947	3219006	3219106	101	2 [1]	[1] 2	nfxB	HTH‑type transcriptional regulator NfxB

CCGATGACCTGCGTCAGGACCTGGTCCCCATAGCTTTCCAGCATGTTCACCAGGTTGTCACGGGTGCCACAGAAACGGTGCAGGGTCGCCTTGCTCACGCCCGCCGCCTCGGCCAGCTCCTTCAATGTGGCTCGGGGGTGGACGACGATCGCG  >  NC_002947/3219104‑3219256    |                                                                                                                                                      ccGATGACCTGCGTCAGGACCTGGTCCCCATAGCTTTCCAGCATGTTCACCAGGTTGTCACGGGTGCCACAGAAACGGTGCAGGGTCGCCTTGCTCACGCCCGCCGCCTCGGCCAGCTCCTTCAATGTGGCTCGGGGGTGGACGACGATc     >  2:306375/1‑150 (MQ=255)    aTGACCTGCGTCAGGACCTGGTCCCCATAGCTTTCCAGCATGTTCACCAGGTTGTCACGGGTGCCACAGAAACGGTGCAGGGTCGCCTTGCTCACGCCCGCCGCCTCGGCCAGCTCCTTCAATGTGGCTCGGGGGTGGACGACGATcgcg  >  1:95224/1‑150 (MQ=255)    |                                                                                                                                                      CCGATGACCTGCGTCAGGACCTGGTCCCCATAGCTTTCCAGCATGTTCACCAGGTTGTCACGGGTGCCACAGAAACGGTGCAGGGTCGCCTTGCTCACGCCCGCCGCCTCGGCCAGCTCCTTCAATGTGGCTCGGGGGTGGACGACGATCGCG  >  NC_002947/3219104‑3219256

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap: ‑    Deleted base: ‑