Supporting information for Rich et al. (December 11, 2001) Proc. Natl. Acad. Sci. USA, 10.1073/pnas.071042098.


Table 3.

Summary of significant fragments detected by Sawyer permutation method

Allele pair

Location

Length, bp

Alignment offset, bp

Number of sites

P

value

Seq 1

Seq 2

Start in Seq 1

Start in Seq 2

S

*

d

vsp1

vsp6

538

541

47

3

28

128

0.009

vsp1

vsp24

547

547

71

0

37

101

0.008

vsp1

vsp26

535

541

61

6

35

118

0.001

vsp1

vsp27

580

589

66

9

27

134

0.007

vsp2

vsp8

58

58

131

0

60

111

0.000

vsp2

vsp22

583

589

66

6

27

124

0.025

vsp2

vsp24

583

580

66

3

27

127

0.018

vsp3

vsp24

70

70

60

0

29

116

0.027

vsp3

vsp27

58

58

65

0

28

132

0.005

vsp6

vsp3

70

70

60

0

29

115

0.029

vsp6

vsp11

58

58

94

0

43

154

0.000

vsp6

vsp24

58

58

180

0

91

105

0.000

vsp6

vsp26

541

544

47

3

28

124

0.016

vsp6

vsp27

70

70

53

0

25

134

0.021

vsp8

vsp13

193

193

35

0

23

139

0.031

vsp11

vsp3

70

70

60

0

29

129

0.004

vsp11

vsp24

58

58

94

0

43

145

0.000

vsp11

vsp27

70

70

53

0

25

168

0.000

vsp22

vsp1

553

544

74

9

40

107

0.001

vsp22

vsp3

70

70

60

0

29

117

0.024

vsp22

vsp6

58

58

158

0

76

106

0.000

vsp22

vsp11

58

58

94

0

43

142

0.000

vsp22

vsp24

58

58

158

0

76

74

0.000

vsp22

vsp24

463

454

74

9

54

74

0.004

vsp22

vsp24

556

547

99

9

45

74

0.047

vsp22

vsp26

553

550

52

3

29

120

0.017

vsp22

vsp27

70

70

53

0

25

138

0.013

vsp24

vsp27

70

70

53

0

25

137

0.015

vsp26

vsp13

585

582

67

3

28

131

0.006

vspB

vspA

582

576

49

6

30

113

0.026

vspB

vspD

58

58

140

0

65

145

0.000

vspB

vspF

148

148

50

0

24

134

0.033

vspD

vspA

88

88

56

0

24

147

0.008

vspD

vspF

148

148

62

0

32

103

0.043

*The number of sites within the fragment that are polymorphic in the complete alignment but identical among the given pair of alleles.
The total number of discordant sites observed between the pair of alleles with the significant fragment.