Best TWAS P=1.046961e-16 · Best GWAS P=0.0002129893 conditioned to 3.101017e-14
# | 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 | Vom2r35 | alternative polyA | ENSRNOT00000107882 | 0.27 | 0.05 | blup | 1024 | 0.07 | 5.4e-08 | -0.84 | 6.0 | 1.9e-09 | -0.59 | 0.06 | 0.03 | TRUE |
2 | Adipose | Zfp110 | gene expression | ENSRNOG00000031328 | 0.18 | 0.00 | blup | 738 | 0.03 | 1.4e-04 | -1.00 | -6.0 | 1.6e-09 | 0.38 | 0.01 | 0.01 | TRUE |
3 | BLA | Zfp110 | gene expression | ENSRNOG00000031328 | 0.47 | 0.01 | enet | 412 | 0.07 | 1.4e-04 | -0.88 | -6.9 | 7.1e-12 | 0.46 | 0.00 | 0.00 | FALSE |
4 | BLA | Zfp329 | isoform ratio | ENSRNOT00000118816 | 0.30 | -0.01 | enet | 401 | 0.02 | 2.7e-02 | -0.96 | -5.9 | 3.6e-09 | 0.59 | 0.01 | 0.00 | FALSE |
5 | Brain | Zscan18 | gene expression | ENSRNOG00000026861 | 0.42 | 0.01 | blup | 978 | 0.03 | 4.8e-04 | -0.88 | -7.6 | 4.1e-14 | 0.67 | 0.01 | 0.01 | TRUE |
6 | Brain | Zfp329 | isoform ratio | ENSRNOT00000026204 | 0.19 | 0.03 | enet | 176 | 0.04 | 1.0e-04 | 1.89 | 8.0 | 1.1e-15 | -0.30 | 0.04 | 0.06 | FALSE |
7 | Brain | Zfp329 | isoform ratio | ENSRNOT00000118816 | 0.20 | 0.03 | enet | 124 | 0.04 | 9.3e-05 | 1.89 | -8.3 | 1.0e-16 | 0.36 | 0.04 | 0.06 | TRUE |
8 | PL | Zfp329 | isoform ratio | ENSRNOT00000026204 | 0.43 | 0.00 | blup | 752 | 0.04 | 2.8e-04 | 1.90 | 7.7 | 1.7e-14 | -0.56 | 0.00 | 0.00 | FALSE |
9 | PL | Zfp329 | isoform ratio | ENSRNOT00000118816 | 0.43 | 0.00 | blup | 752 | 0.04 | 2.7e-04 | 1.90 | -7.7 | 1.5e-14 | 0.56 | 0.00 | 0.00 | FALSE |
10 | PL | Vom1r50 | intron excision ratio | chr1:72483651:72525014 | 0.18 | 0.00 | blup | 1711 | 0.01 | 7.0e-02 | 1.65 | 5.2 | 2.1e-07 | -0.80 | 0.23 | 0.17 | FALSE |
11 | PL | NA | intron excision ratio | chr1:72483651:72525014 | 0.18 | 0.00 | blup | 1711 | 0.01 | 7.0e-02 | 1.65 | 5.2 | 2.1e-07 | -0.80 | 0.23 | 0.17 | 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.