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. 2016 Jun 7;6:27296. doi: 10.1038/srep27296

Table 2. Putative selective sweeps identified in the hapFLK-based analysis.

CHR Reg (Mb) Flanking SNPs of SNPs Number Raw P-value q-value Gutiérrez-Gil et al.8 Fariello et al.7
2 82.8–87.7 OAR2_88062818.1–s35257.1 97 0.034 0.574 83.1–85.3 Mb 81.2–87.3 Mb
3 150.5154.2 s26286.1OAR3_165050963.1 68 0.029 0.545 153.4–154.5 Mb 151.4–156.9 Mb
5 46.5–49.1 s59995.1–OAR5_53435489.1 48 0.007 0.213 47.3–49.3 Mb
6 4.349.9 OAR6_6402059.1OAR6_55087517_X.1 860 0.000 0.000 39.3–39.5 Mb 35.9–38.3 Mb
52.3–52.6 OAR6_57796972.1–OAR6_58069886.1 7 0.049 0.604
64.5–74.3 OAR6_70844973.1–OAR6_81183719.1 180 0.016 0.389 69.9–70.5 Mb 67.9–70.3 Mb
112.1–115.6 OAR6_127397796.1–s33220.1 58 0.026 0.52
10 29.1–29.3 OAR10_29159858.1–OAR10_29381795.1 7 0.044 0.598 29.4–29.7 Mb
13 43.6–50.9 s39429.1–OAR13_55448085.1 104 0.006 0.192 48.9–52.0 Mb 43.3–51.2
68.874.9 OAR13_74074760.1OAR13_80614774_X.1 97 0.025 0.524
16 24.7–25.2 s59907.1–OAR16_27501072.1 13 0.043 0.598
17 61.2–67.1 s25636.1–s73670.1 34 0.039 0.591
24 6.9–11.0 OAR24_8063846.1–s18520.1 44 0.042 0.598
25 24.8–45.3 OAR25_25923466.1–OAR25_48288071_X.1 353 0.008 0.249
26 0.16–3.8 OAR26_222715_X.1–s54858.1 47 0.030 0.547

Those sweeps consistently found with BayeScan are shown in bold.

In the two columns at the right part of the table, we show evidence of positional concordance with previously reported selective sweeps7,8. CHR = chromosome.