Best TWAS P=6.859554e-08 · Best GWAS P=9.203324e-08 conditioned to 0.286555
# | Tissue | Gene | Modality | RNA phenotype | h2 | eQTL R2 | model | # weights | model R2 | model R2 P | eQTL GWAS Z | TWAS Z | TWAS P | Top SNP corr | PP3 | PP4 | joint |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | Adipose | Ivd | alternative polyA | ENSRNOT00000107497 | 0.19 | 0.10 | enet | 158 | 0.10 | 1.3e-11 | 4.6 | -5.1 | 3.3e-07 | -0.68 | 0.59 | 0.41 | FALSE |
2 | Adipose | Ivd | alternative polyA | ENSRNOT00000013829 | 0.19 | 0.10 | enet | 177 | 0.10 | 2.5e-11 | 4.6 | 5.2 | 2.5e-07 | 0.73 | 0.60 | 0.40 | FALSE |
3 | Adipose | NA | gene expression | ENSRNOG00000012290 | 0.11 | 0.04 | enet | 310 | 0.04 | 1.6e-05 | 5.1 | -5.2 | 2.6e-07 | -0.92 | 0.11 | 0.88 | FALSE |
4 | BLA | Ehd4 | gene expression | ENSRNOG00000007584 | 0.32 | 0.23 | lasso | 5 | 0.23 | 1.4e-12 | 4.8 | -5.4 | 6.9e-08 | -0.91 | 0.30 | 0.70 | TRUE |
5 | Brain | Ehd4 | gene expression | ENSRNOG00000007584 | 0.32 | 0.24 | lasso | 9 | 0.26 | 2.1e-24 | 5.2 | -5.2 | 1.7e-07 | -0.92 | 0.15 | 0.85 | FALSE |
6 | Brain | Mapkbp1 | mRNA stability | ENSRNOG00000007018 | 0.08 | 0.08 | top1 | 1 | 0.08 | 3.9e-08 | 5.1 | -5.1 | 2.9e-07 | -0.93 | 0.22 | 0.78 | FALSE |
7 | Brain | Ehd4 | mRNA stability | ENSRNOG00000007584 | 0.10 | 0.10 | top1 | 1 | 0.10 | 2.7e-09 | 5.2 | -5.2 | 1.8e-07 | -0.92 | 0.13 | 0.87 | FALSE |
8 | Liver | Disp2 | gene expression | ENSRNOG00000026787 | 0.04 | 0.03 | top1 | 1 | 0.03 | 5.8e-04 | 5.2 | -5.2 | 1.9e-07 | -0.97 | 0.06 | 0.19 | FALSE |
9 | NAcc2 | Ganc | mRNA stability | ENSRNOG00000024563 | 0.08 | 0.04 | lasso | 2 | 0.04 | 3.6e-03 | 4.7 | -5.1 | 2.8e-07 | -0.86 | 0.27 | 0.48 | FALSE |
10 | PL2 | Sptbn5 | intron excision ratio | chr3:107017537:107018049 | 0.12 | 0.07 | top1 | 1 | 0.07 | 1.6e-04 | 5.1 | -5.1 | 3.0e-07 | -0.88 | 0.10 | 0.27 | FALSE |
h2: Heritability estimate for the given transcriptomic model. PP3: Posterior probability of two distinct causal variants. PP4: Posterior probability of a single shared causal variant. joint: Whether the RNA phenotype is in the joint model.