Table 3.
Chr | Position (build 37) | CpG | Mapped gene | Gene group | Coef | SE | p-Value | Direction |
---|---|---|---|---|---|---|---|---|
11 | 34460856 | cg03728580 | CATFDR | Body | 0.003 | 0.001 | 0.00001 | ++++ |
11 | 34461028 | cg17034036 | CATFDR | Body | 0.002 | 0.001 | 0.0001 | ++++ |
2 | 1482597 | cg01385533 | TPOFDR | Body | –0.003 | 0.001 | 0.0004 | –?–– |
1 | 226023590 | cg05935800 | EPHX1 | Body | –0.002 | 0.001 | 0.002 | –––– |
20 | 33539306 | cg13607138 | GSS | Body | –0.003 | 0.001 | 0.003 | ––?– |
8 | 107642385 | cg17526936 | OXR1 | Body | –0.002 | 0.001 | 0.004 | ––?– |
2 | 1544120 | cg19407717 | TPO | Body | –0.002 | 0.001 | 0.004 | –––– |
2 | 1479523 | cg13703866 | TPO | Body | –0.001 | 0.000 | 0.005 | –––– |
11 | 34460336 | cg07768201 | CAT | TSS200 | 0.003 | 0.001 | 0.006 | ++++ |
1 | 226012507 | cg03337430 | EPHX1 | TSS1500;5’UTR | 0.001 | 0.000 | 0.006 | +–++ |
Shown are the top 10 CpGs ordered by p-value. Three CpGs were statistically significant using genome-wide significance threshold (FDR p < 0.05). Results presented per 10 μg/m3 increase in prenatal NO2 exposure. Column heads: Chr: chromosome; Position: chromosomal position based on NCBI human reference genome assembly Build 37. Mapped Gene: UCSC annotated gene; Gene group: UCSC gene region feature category; Coef: regression coefficient; SE: standard error for regression coefficient; Direction: direction of effect across cohorts included in the statistical model (MeDALL, Generation R, CHS, and MoBa): NO2 exposure during pregnancy associated with increased (+) or decreased (–) methylation, or missing (?) result. |