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. 2010 May 5;27(10):2284–2299. doi: 10.1093/molbev/msq114

Table 1.

Population Genetic Summary Statistics for Independently Evolving Regions of eater.

n h S bp π πns πs Tajima's D ZnS
Zimbabwe
    Entire gene 10 9 142 3895 0.01188 0.00367 0.02075 −0.5199 0.1321
    5' gene region 10 9 123 3213 0.01271 0.00356 0.01934 −0.4621 0.1341
    Intron 2 10 8 30 398 0.02903 n/a n/a 0.2622 0.1796
New York
    Entire gene 18 16 94 3895 0.00768 0.00343 0.00654 0.2665 0.1462
    5' gene region 18 16 86 3213 0.00861 0.00345 0.00862 0.2906 0.1560***
    Intron 2 18 5*** 15 398 0.01867*** n/a n/a 2.6697*** 0.7474*
New York (“A” group)
    Entire gene 8 6 64 3895 0.00564 0.00386 0.00589 −0.7286 0.2987
    5' gene region 8 6** 59 3213 0.00635 0.00434 0.00913 −0.7129*** 0.312***
    Intron 2 8 2* 3 398 0.00188** n/a n/a −1.4475* 1*
New York (“B” group)
    Entire gene 10 10 56 3895 0.00477 0.00284 0.00493 −0.3730 0.187
    5' gene region 10 10 49 3213 0.00499 0.00285 0.00509 −0.4352 0.1869
    Intron 2 10 3 4 398 0.00201 n/a n/a −1.6671 0.5062

NOTE.—n/a, not applicable; n, number of alleles sampled; h, number of haplotypes; S, segregating sites; bp, sequence length in base pairs; π is nucleotide diversity per base pair; ns, nonsynonymous; s, synonymous. The US population was both analyzed as a whole and split into haplotype groups. Tajima's D (Tajima 1989) includes all mutations. ZnS (Kelly 1997) is linkage disequilibrium based on segregating sites. Statistically significant values (*0.01 ≤ P < 0.05; **0.001 ≤ P < 0.01; ***P < 0.001) under a null demographic model are indicated (*) for the 5′ gene region and intron 2 in the New York population and the “A” haplotype group (see table 2).