Table 5 of Fink, Mol Vis 2012; 18:2229-2240.
SNP ID | Chromosome - position (bp) | χ2 allele | p allele | χ2 genotype | p genotype | χ2 trend | p trend |
---|---|---|---|---|---|---|---|
Hapmap42731-BTA-92931 | 5–21768260 | 2.34 | 0.126 | 4.64 | 0.098 | 2.26 | 0.132 |
ARS-BFGL-NGS-12640 | 5–23861315 | 6.73 | 0.010 | 8.07 | 0.017 | 6.36 | 0.011 |
DN825458:c.168G>T* | 5–24073205 | 17.18 | <0.001 | 20.64 | <0.001 | 19.24 | <0.001 |
XM_596354:c.1678A>G* | 5–24142953 | 0.54 | 0.460 | 0.59 | 0.742 | 0.54 | 0.461 |
EH152007:c.462T>C* | 5–24215836 | <0.001 | 0.996 | 0.60 | 0.739 | <0.001 | 0.996 |
Hapmap41951-BTA-73168 | 5–28442563 | 0.17 | 0.681 | 0.62 | 0.732 | 0.18 | 0.673 |
BTA-73209-no-rs | 5–29496625 | 1.35 | 0.243 | 2.60 | 0.272 | 1.45 | 0.228 |
ARS-BFGL-NGS-49972 | 5–30012017 | 3.20 | 0.07 | 3.81 | 0.149 | 3.46 | 0.063 |
AM931450:c.205T>G* | 5–42079372 | 2.48 | 0.115 | 2.90 | 0.235 | 2.88 | 0.090 |
ARS-BFGL-NGS-93837 | 18–55807264 | 0.91 | 0.338 | 1.85 | 0.396 | 0.98 | 0.321 |
AM930539:g.569A>G+ | 18–56565243 | 2.17 | 0.141 | 2.26 | 0.323 | 2.07 | 0.150 |
Hapmap42211-BTA-43910 | 18–58203733 | 2.38 | 0.123 | 2.58 | 0.108 | 2.58 | 0.108 |
ARS-BFGL-BAC-31654 | 18–62250437 | 1.38 | 0.238 | 1.74 | 0.419 | 1.36 | 0.242 |
ARS-BFGL-NGS-1786 | 18–62571431 | 0.14 | 0.702 | 0.67 | 0.715 | 0.16 | 0.692 |
AM930544:g.71G>A+ | 18–62704882 | 1.87 | 0.172 | 3.86 | 0.146 | 1.94 | 0.163 |
AM930553:c.703C>A+ | 18–62800146 | 9.24 | 0.005 | 9.22 | 0.002 | 8.95 | 0.003 |
AM930547:g.194C>T+ | 18–62800898 | 8.06 | 0.006 | 8.42 | 0.015 | 8.15 | 0.004 |
AM930543:g.103T>G+ | 18–62878596 | 6.18 | 0.013 | 7.15 | 0.028 | 5.88 | 0.015 |
ARS-BFGL-NGS-41595 | 18–63400996 | 0.01 | 0.900 | 0.04 | 0.979 | 0.01 | 0.903 |