Missing coverage evidence...
   seq id start end size ←reads reads→ gene description
* * ÷ REL606 2031674–2031721 2054972–2054943 23223–23299 20 [15] [15] 16 [manB]–[cpsG] 23 genes
[manB], manC, insB‑14, insA‑14, wbbD, wbbC, wzy, wbbB, wbbA, vioB, vioA, wzx, rmlC, rfbA, rfbD, rfbB, galF, wcaM, wcaL, wcaK, wzxC, wcaJ, [cpsG]

TCACCGCTTGCCGGAAACGCCGCCATCCGGTCACGTACCAGTTCG  >  REL606/2054964‑2055008
         |                                   
tcACCGCTAGCCCGAAACGCCGCCATCCGGCCACGt           >  2:1068260/1‑36 (MQ=14)
cccccGTTTGCCGGAAACGCCGCCATCCGGTCACGt           <  2:1642350/33‑1 (MQ=14)
 cACCGCTTGCCGGAAACGCAGCCATCCGGTCACGTa          >  2:2009861/1‑36 (MQ=255)
  aCCGCTTGCCGGAAACGCCGCCATCCGGTCACGTAc         >  1:1462581/1‑36 (MQ=255)
   ccGCTTCCCGGAAACGCCCCCATCCGGTCACGTAcc        <  2:673544/36‑1 (MQ=17)
   ccGCTCGCCGAAAACGCCGCCATCCGGTCACGTAcc        <  1:3247921/36‑1 (MQ=17)
    cGCTTGCCGGAAACGCCGCCATCCGGTCACGTACCa       >  1:100870/1‑36 (MQ=255)
     gCTTGCCGGAAACGCCGCCATCCGGTCACGTACCAg      <  1:642054/36‑1 (MQ=255)
     gCTTGCCGGAAACGCCGCCATCCGATCACGAACCAg      >  2:2963400/1‑36 (MQ=14)
      cTTGCGGAAAACGCCGCCATCCGGTCACGTACCAGt     <  2:540952/36‑1 (MQ=17)
      cTTGCCGGAAACGCCGCCATCCGGTCACGTACCAGt     >  1:3034769/1‑36 (MQ=255)
      cTTGCCGGAAACGCCGCCATCCGGTCACGTACCAGt     >  2:949406/1‑36 (MQ=255)
       ttGCCGGAAACGCCGCCATCCGGTCACGTACGAGtt    >  1:3150936/1‑36 (MQ=255)
       ttGCCGGAAACGCCGCCATCCGGTCACGTACCAGtt    <  1:429197/36‑1 (MQ=255)
       ttGCCGGAAACGCCGCCATCCGGCCACGTACCAGtt    >  1:565482/1‑36 (MQ=255)
         gCCGGAAACGCCGCCATCCGGTCACGTACCAGTTCg  >  2:895390/1‑36 (MQ=255)
         |                                   
TCACCGCTTGCCGGAAACGCCGCCATCCGGTCACGTACCAGTTCG  >  REL606/2054964‑2055008

Base quality scores:  ATCG  < 3 ≤  ATCG  < 5 ≤  ATCG  < 10 ≤  ATCG  < 26 ≤  ATCG  < 32 ≤  ATCG