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. 2015 Dec 9;5:17950. doi: 10.1038/srep17950

Table 2. Sequence variants in the EnhII/BCP/PC regions of HBeAg-positive CHB patients.

    Total Genotype C Genotype B  
Region Variant (n = 58) (%) (n = 40) (%) (n = 18) (%) Pvalue
EnhII G1719T 28 (48.3) 24 (60.0) 4 (22.2) 0.0107
(1685–1773) A1726C 18 (31.0) 3 (7.5) 15 (83.3) <.0001
  A1727Vc (T1727Vb) 30 (51.7) 24 (60.0) 6 (33.3)  
BCP G1746A 56 (96.6) 39 (97.5) 17 (94.4) 0.5281
(1742–1849) A1752G/T 17 (29.3) 3 (7.5) 14 (77.8) <.0001
  T1753V 22 (37.9) 20 (50.0) 2 (11.1) 0.0075
A1762T 35 (60.3) 28 (70.0) 7 (38.9) 0.0413
G1764A 35 (60.3) 28 (70.0) 7 (38.9) 0.0413
PC C1817G/A 18 (31.0) 11 (27.5) 7 (38.9) 0.5404
(1814–1900) T1825C/A 58 (100.0) 40 (100.0) 18 (100.0)  
  A1846T 19 (32.8) 10 (25.0) 9 (50.0) 0.0757
G1896A 29 (50.0) 18 (45.0) 11 (61.1) 0.3950

For all nucleotide positions in EnhII/BCP/PC regions, the most prevalent nucleotide type among HBV genotype B or genotype C infection patients in china were used as reference nucleotide. EnhII, enhancer II; BCP, basal core promoter; PC, precore; cGenotype C; bGenotype B; A, adenine; G, guanine; C, cytosine; T, thymine. Data presented as no. (%). P, Fisher’s exact test.