Table 1.
BTA | SNP name | Position (bp) | MAF | BF | Candidate QTL | Allele subs. effecta | Number of candidate genes | Total genetic var. expl. (%) |
---|---|---|---|---|---|---|---|---|
1 | BTA89822nors | 46223040 | 0.491 | 14.33 | Yes | 0.113 | 12 | 0.006 |
1 | BTA89820nors | 46321775 | 0.488 | 12.26 | 0.193 | |||
4 | Hapmap39581BTA70101 | 9203380 | 0.497 | 12.26 | Yes | 0.226 | 14 | 0.003 |
4 | ARSBFGLNGS109843 | 9615916 | 0.430 | 14.33 | 0.251 | |||
9 | BTB00395654 | 60102040 | 0.353 | 32.29 | — | 0.132 | 1 | 0.003 |
9 | ARSBFGLNGS36482 | 64262480 | 0.365 | 16.41 | Yes | 0.201 | 9 | 0.005 |
9 | BTB01673493 | 64291804 | 0.365 | 16.41 | 0.172 | |||
9 | Hapmap42513BTA33276 | 66997852 | 0.215 | 23.76 | Yes | 0.183 | 7 | 0.005 |
9 | Hapmap27624BTA154889 | 67122449 | 0.318 | 13.29 | 0.158 | |||
13 | BPI1 | 67833218 | 0.402 | 11.22 | Yes | 0.144 | 21 | 0.003 |
13 | ARSBFGLNGS103635 | 67888763 | 0.467 | 48.68 | 0.152 | |||
20 | ARSBFGLNGS109784 | 909076 | 0.407 | 36.61 | — | 0.129 | 1 | 0.003 |
25 | ARSBFGLNGS61709 | 1086505 | 0.432 | 17.45 | Yes | 0.277 | 65 | 0.004 |
25 | ARSBFGLNGS103099 | 1127441 | 0.395 | 15.37 | 0.238 | |||
25 | ARSBFGLBAC43143 | 1184038 | 0.395 | 24.82 | 0.101 | |||
25 | Hapmap29768BTC016149 | 1205232 | 0.346 | 16.41 | 0.321 |
aAllele substitution effects were estimated as , where is the genetic variance explained by the SNP, and p and q are the frequencies of the two alleles76.