Table 2.
CpG Name | Chromosome | Nearby Gene(s) |
USCS RefGene Group |
Univariate (0 sites identified) |
HIMA (3 sites identified) |
HDMA (11 sites identified) |
MedFix (3 sites identified) |
Pathway LASSO (141 sites identified) |
BSLMM (3 sites identified) |
---|---|---|---|---|---|---|---|---|---|
cg10508317 | 17 | SOCS3 | Body | 3.48 x10−2 | 1.59 x10−2* | 3.56 x10−2* | 2.90 x10−2* | 2.35 x10−2* | 0.25 x10−2 |
cg01288337 | 14 | RIN3 | Body | 3.35 x10−2 | 1.47 x10−2* | 2.82 x10−2* | 2.70 x10−2* | 4.43 x10−2* | 0.21 x10−2 |
cg10244976 | 16 | LMF1 | Body | 3.00 x10−2 | 0 | 2.78 x10−2* | 0 | 2.23 x10−2* | 0.19 x10−2 |
cg07516252 | 14 | REC8 | TSS200 | 2.72 x10−2 | 0 | 2.24 x10−2* | 0 | 2.26 x10−2* | 0.26 x10−2 |
cg07571519 | 10 |
C10orf105; CDH23 |
3'UTR; Body | 2.53 x10−2 | 0.33 x10−2* | 3.67 x10−2* | 1.47 x10−2* | 2.81 x10−2* | 0.21 x10−2 |
cg23079012 | 2 | LINC00299 | Body | 2.27 x10−2 | 0 | 1.99 x10−2* | 0 | 1.98 x10−2* | 0.29 x10−2 |
cg01587454 | 8 | DCAF4L2 | 1stExon | 1.77 x10−2 | 0 | 2.10 x10−2* | 0 | 1.99 x10−2* | 0.38 x10−2 |
cg27527503 | 4 | HADH | TSS1500 | 1.75 x10−2 | 0 | 1.86 x10−2* | 0 | 1.27 x10−2* | 0.23 x10−2 |
cg25891647 | 11 | GRAMD1B | Body | −1.27 x10−2 | 0 | −3.42 x10−2* | 0 | −3.02 x10−2* | −0.33 x10−2 |
cg08473752 | 17 | NLK | Body | −0.70 x10−2 | 0 | −2.34 x10−2* | 0 | −2.32 x10−2* | −0.22 x10−2 |
cg12644059 | 15 | BLM | N/A1 | −0.03 x10−2 | 0 | −2.31 x10−2* | 0 | −1.84 x10−2* | −0.22 x10−2 |
Selected as noteworthy by given method
CpG site cg12644059 is 3.240kb from the final base pair of the BLM gene
Table includes all CpG sites that were selected as having a noteworthy mediation contribution by at least two of the implemented methods out of 2,000 CpG sites in total. Criteria for CpG identification varied by method. All estimates are adjusted for age, sex, race, and the estimated proportions of residual non-monocytes as fixed effects, along with methylation chip and position as random effects to address potential batch effects. Note that for HIMA, HDMA, MedFix, and pathway LASSO, which fit high-dimensional regression models, we used additional pre-screening to reduce the number of mediators in advance to only n/log(n) ≈ 141 CpG sites, which is the approach recommended by the HIMA and HDMA authors and helps with statistical and computational efficiency (see Methods). Pathway LASSO selected all of these 141.