Table 4.
Contribution of SNPs on the genome-wide significant region for ESS36 and ESS46.
| Traits | Chromosome | Position (start–end) | No. of SNP | CPV (%) |
|---|---|---|---|---|
| ESS36 | 1 | 175,916,717 – 176,057,617 | 41; 22 | 0.0223 |
| ESS36 | 3 | 39,043,602 | 11 | 0.1023 |
| ESS36 | 13 | 8,733,921 | 12 | 0.3514 |
| ESS36 | 14 | 2,902,989–3,009,565 | 52 | 0.0005 |
| ESS46 | 1 | 22,759,904 – 23,708,413 | 11; 312 | 9.5855 |
| ESS46 | 15 | 7,289,187 | 12 | 0.0001 |
Chromosome, chicken chromosome; CPV, contribution to phenotypic variance (%); Position(start∼end), the start and the end of the genome-wide significant region. No. of SNP, the number of the SNPs.
1
SNPs reached genome-wide significant level (P value < 4.48E-06).
2
SNPs reached the genome-wide suggestive threshold (P value < 8.97E-05).