Best TWAS P=8.127602e-12 · Best GWAS P=7.395848e-12 conditioned to 1
# | 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 | Brain | Pclo | alternative polyA | ENSRNOT00000007608 | 0.08 | 0.03 | lasso | 6 | 0.04 | 2.3e-04 | -6.1 | -5.9 | 3.4e-09 | 0.88 | 0.32 | 0.62 | FALSE |
2 | Brain | Pclo | alternative polyA | ENSRNOT00000008637 | 0.08 | 0.03 | lasso | 6 | 0.04 | 1.9e-04 | -6.1 | 5.9 | 4.2e-09 | -0.88 | 0.33 | 0.61 | FALSE |
3 | Brain | Cacna2d1 | gene expression | ENSRNOG00000033531 | 0.05 | 0.06 | top1 | 1 | 0.06 | 5.7e-06 | -6.8 | -6.8 | 8.1e-12 | 0.99 | 0.40 | 0.47 | TRUE |
4 | Brain | Pclo | isoform ratio | ENSRNOT00000007608 | 0.05 | 0.01 | enet | 29 | 0.03 | 1.0e-03 | -5.6 | -5.9 | 3.6e-09 | 0.73 | 0.39 | 0.48 | FALSE |
5 | Brain | Pclo | isoform ratio | ENSRNOT00000008637 | 0.05 | 0.01 | enet | 30 | 0.03 | 5.5e-04 | -5.6 | 5.8 | 5.8e-09 | -0.70 | 0.40 | 0.50 | FALSE |
6 | Brain | Pclo | mRNA stability | ENSRNOG00000005726 | 0.28 | 0.19 | enet | 64 | 0.24 | 4.1e-22 | -5.0 | 5.6 | 1.9e-08 | -0.92 | 0.81 | 0.19 | FALSE |
7 | IL | Hgf | gene expression | ENSRNOG00000007027 | 0.45 | 0.31 | enet | 18 | 0.34 | 6.6e-09 | 4.4 | -5.2 | 2.4e-07 | 0.71 | 1.00 | 0.00 | FALSE |
8 | LHb | Pclo | intron excision ratio | chr4:19838555:19842972 | 0.18 | 0.05 | enet | 6 | 0.05 | 2.9e-02 | -4.8 | -5.5 | 4.9e-08 | 0.89 | 0.38 | 0.22 | FALSE |
9 | NAcc | Cacna2d1 | gene expression | ENSRNOG00000033531 | 0.21 | 0.07 | top1 | 1 | 0.07 | 1.2e-02 | -6.8 | -6.8 | 1.5e-11 | 0.99 | 0.13 | 0.05 | FALSE |
10 | PL2 | NA | gene expression | ENSRNOG00000070617 | 0.35 | 0.42 | blup | 2612 | 0.42 | 8.1e-25 | 4.5 | 5.3 | 1.1e-07 | -0.77 | 1.00 | 0.00 | 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.