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. 2007 Oct;177(2):1071–1085. doi: 10.1534/genetics.106.069468

TABLE 2.

Nucleotide variation in two populations of D. melanogaster

Zimbabwe
China
Region Length Description n Div S H D n S H D
1302 987 5′ NCa 12 108 10 −0.89 +0.18 12 2 +1.20 −0.96
3303 1012 5′ NCa 12 79 18 +0.15 −0.91 12 4 −0.98 −1.33
5089 983 5′ NCa 12 61 8 +0.97 −1.12 12 0 NA NA
6072 917 dm exon1 12 83 8 −0.37 −1.31 12 0 NA NA
7324 988 Intron 12 101 7 +0.18 −0.97 12 0 NA NA
9807 1003 Intron 12 78 10 +0.22 −0.66 12 0 NA NA
15987 1016 Intron 12 95 27 −3.98* −0.43 12 0 NA NA
17003 1002 dm exon2 28 80 34 −12.32* −0.22 12 4 +1.20 −0.22
19004 904 3′ NCa 12 48 23 −1.12 −0.87 12 4 −1.12 −0.32
21332 987 CG12535 12 163 29 −0.99 +1.1 12 3 −0.54 −1.98

The region's starting point, length of sequence, type of region (noncoding, exon, and intron), sample size (n), number of pairwise differences when comparing against D. simulans (Div), and number of segregating sites (S) for each population, as well as the relative values of Fay and Wu's H and Tajima's D, respectively, are shown. *Significance after Bonferonni correction.

a

Noncoding.