Table 3.
Full genome | pre‐S1 | pre‐S2 | S | pre‐C/core | X | Pol | Enhancer I | Enhancer II | X promoter | core promoter | S1 promoter | S2 promoter | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
(nt 0–3215) | (nt 2484–3204) | (nt 3205–154) | (nt 155–835) | (nt 1814–2452) | (nt 1376–1846) | (nt 2307–1620) | (nt 1060–1260) | (nt 1635–1714) | (nt1230–1376) | (nt 1519–1822) | (nt 2710–2800) | (nt 2960–3180) | |
Non‐HCC group (B) | 68.35 ± 20.90 | 9.15 ± 3.73 | 4.40 ± 2.19 | 5.30 ± 2.16 | 10.30 ± 5.40 | 9.05 ± 3.25 | 54.55 ± 15.51 | 8.15 ± 3.05 | 1.70 ± 0.92 | 6.10 ± 1.99 | 5.30 ± 2.70 | 1.75 ± 1.12 | 7.95 ± 3.07 |
Non‐HCC group (A) | 71.85 ± 21.64 | 9.75 ± 3.58 | 4.65 ± 2.28 | 6.05 ± 2.19 | 12.55 ± 5.67 | 8.90 ± 2.56 | 56.30 ± 16.70 | 7.65 ± 2.70 | 1.60 ± 0.88 | 6.05 ± 1.88 | 5.35 ± 1.93 | 1.85 ± 1.50 | 8.20 ± 2.89 |
HCC group (B) | 76.13 ± 11.59 | 10.26 ± 2.14 | 3.78 ± 1.93 | 5.74 ± 1.60 | 13.00 ± 5.75 | 9.69 ± 1.87 | 59.04 ± 8.23 | 8.09 ± 2.15 | 1.83 ± 0.98 | 7.26 ± 1.66 | 5.48 ± 1.44 | 1.78 ± 0.85 | 9.04 ± 1.36 |
HCC group (A) | 80.26 ± 17.74 | 10.61 ± 2.87 | 4.39 ± 2.43 | 6.52 ± 3.87 | 14.52 ± 6.49 | 9.91 ± 2.71 | 61.65 ± 13.14 | 7.96 ± 1.99 | 1.70 ± 0.82 | 7.04 ± 1.92 | 5.43 ± 1.56 | 2.26 ± 1.39 | 9.61 ± 2.02 |
P (non‐HCC B vs HCC B) | 0.14 | 0.27 | 0.55 | 0.47 | 0.18 | 0.21 | 0.23 | 0.81 | 0.62 | 0.07 | 0.66 | 0.87 | 0.16 |
P (non‐HCC A vs HCC A) | 0.20 | 0.57 | 0.43 | 0.61 | 0.25 | 0.39 | 0.31 | 0.75 | 0.95 | 0.06 | 0.88 | 0.35 | 0.12 |
The significance of differences (P‐value) in the indicated groups is shown. The number of nucleotide (nt) substitutions (mean±SD) in the full genome and the indicated regions of HBV are shown. Non‐HCC group (B): at the beginning of follow‐up in patients who did not develop HCC. Non‐HCC group (A): at the end of follow‐up in patients who did not develop HCC. HCC group (B): at the beginning of follow‐up in patients who developed HCC. HCC group (A): at the diagnosis of HCC in patients who developed HCC.