TABLE 1

Polymorphism data for human data sets

Locus	n^{^a}	Bps	S^{^b}	π (%)^{^c}	D*^{^d}	D^{^e}	C_HRM^{^f}	Source
Lpl	142	9700	87	0.190	0.926	0.542	115^{^g}	Clark et al. (1998)
Ace	22	24000	78	0.098	−0.286	0.391	17	Rieder et al. (1999)
Dys44	250	7622	34	0.093	—^{^h}	0.744	—^ⁱ	Zietkiewicz et al. (1998)
Xq13.3	70	10163	33	0.033	−3.346^{^j}	−1.616	1.8	Kaessmann et al. (1999)
Pdha1	35	4194	24	0.178	0.851	0.973	6.2	Harris and Hey (1999)
Duffy^{^k}	82	1931	22	0.128	0.188	−0.449	—^{^l}	Hamblin and Di Rienzo (2000)
Dmd44^{^m}	41	3000	17	0.136	−0.366	0.089	68	Nachman and Crowell (2000)
β-globin	349	2670	19	0.157	−0.593	1.058	21	Harding et al. (1997)
Dmd7^{^l}	41	2389	12	0.051	−2.631^{^j}	−1.725^{^j}	—^{^l}	Nachman and Crowell (2000)
zfx	336	1089	10	0.082	0.469	−0.938	3.7	Jaruzelska et al. (1999)
Mc1r	242	951	6	0.114	−1.063	0.195	0.5	Rana et al. (1999)
Hprt	10	2485	4	0.038	−1.127	−1.245	1.0	Nachman et al. (1998)

↵^a Sample size.
↵^b Number of segregating sites.
↵^c Average number of pairwise differences per base pair, in percentage (cf. Tajima 1983).
↵^d From Tajima (1989a).
↵^e From Fu and Li (1993).
↵^f Sequence-based estimate of the rate of recombination per locus.
↵^g These values are probably underestimates since available phase information was incomplete.
↵^h Could not be calculated because the data from the original ascertainment sample are unavailable.
↵ⁱ Could not be calculated because haplotype information is unavailable.
↵^j P < 0.05 (two tailed). Coalescent simulations with no recombination were used to assess significance levels.
↵^k Includes both Duffy and the noncontiguous 5′ region sequenced.
↵^l Sequence not contiguous.
↵^m This region is in the same intron as Dys44.