Table 1.
Set | ntotal | perceQTL_all | FDR | nsignCI | perceQTL_CI | Enrichment | penrichment |
---|---|---|---|---|---|---|---|
All | 13,710,843 | – | – | 3412 | 0.02a | – | – |
GE | 1,196,131 | 8.72a | 7.5 × 10–5 | 1719 | 50.38b | 5.8 | 0 |
EE | 1,019,185 | 7.43a | 1.4 × 10–4 | 2117 | 62.05b | 8.3 | 0 |
S | 2,019,663 | 14.73a | 2.5 × 10–4 | 813 | 23.83b | 1.4 | 4.5 × 10–26 |
ASE | 305,494 | 2.23a | 4.4 × 10–4 | 604 | 17.70b | 7.9 | 0 |
FDR GWAS false discovery rate, ntotal total number of variants included in set, nsignCI number of variants significantly associated with calving interval (CI), GE variants significantly associated with gene expression, EE variants significantly associated with exon expression, S variants significantly associated with gene splicing, ASE variants significantly associated with allele specific expression, expressed in % of the 13,7 M variants included in the GWAS for CIa, or the 3412 variants significantly associated with CIb, enrichment = perceQTL_CI/perceQTL_all, penrichment = p-value of the Chi-square test enrichment