SNPs for HTDMY_slope and THI_slope validated in the Jersey data set and their effects in the discovery and validation data set.

The effects are the result of inheriting one extra copy of the second allele of the SNP (alleles in alphabetical order and called in top-bottom format). The F-value thresholds were 10.84 (P<0.001) for discovery and 3.85 (P<0.05) for validation. Blank cells indicate non-significance. *Note that the ARS prefix in front of BFGL in the marker names has been removed for clarity.