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. 2021 Sep 15;31(4):651–664. doi: 10.1093/hmg/ddab274

Table 1.

CpG sites associated with phenotypes in either MWAS 1 or MWAS 2

Phenotype CpG site Chr BP position Annotated Gene MWAS 1 MWAS 2
Effect size Standard error P-value Effect size Standard error P-value
Preterm birth cg00725333 3 64 189 256 PRICKLE2 −0.2747 0.0376 6.24 × 10 −13 −0.0364 0.0060 1.15 × 10 −9
cg17668848 3 108 029 973 HHLA2 −0.2871 0.0396 9.13 × 10 −13 −0.0356 0.0058 8.21 × 10 −10
cg24329141 10 27 095 369 ABI1 −0.2368 0.0352 2.98 × 10 −11 −0.0345 0.0057 1.27 × 10 −9
Low birth weight cg15582176 1 1 183 528 C1QTNF12 −0.3604 0.0661 6.53 × 10 −8 −0.0254 0.0054 2.49 × 10−6
cg19909717 6 107 924 415 SOBP −0.2225 0.0403 4.35 × 10 −8 −0.0329 0.0055 1.59 × 10 −9
cg21803443 7 126 547 786 GRM8 −0.3656 0.0618 4.62 × 10 −9 −0.0278 0.0056 7.22 × 10−7
cg12090821 14 21 755 658 RPGRIP1 −0.0857 0.0152 2.43 × 10 −8 −0.0329 0.0058 1.47 × 10 −8
cg05905731 16 85 485 785 −0.1695 0.0300 2.23 × 10 −8 −0.0294 0.0055 7.50 × 10−8
Young parent cg00528572 11 92 703 433 MTNR1B −0.1369 0.0200 9.04 × 10 −12 −0.0145 0.0025 4.47 × 10 −9
cg02427109 18 77 917 459 PARD6G, PARD6G-AS1 −0.1163 0.0213 4.96 × 10 −8 −0.0101 0.0025 4.12 × 10−5
Population density cg06759845 1 156 460 474 MEF2D 5.20 × 10−6 9.40 × 10−7 3.40 × 10 −8 90.39 17.02 1.10 × 10−7
cg12433043 6 100 619 893 −6.65 × 10−6 1.20 × 10−6 3.37 × 10 −8 −88.86 16.75 1.13 × 10−7
cg03623878 13 113 655 560 MCF2L 9.10 × 10−6 1.58 × 10−6 9.56 × 10 −9 81.18 16.88 1.51 × 10−6
cg08036492 17 13 976 536 COX10 3.09 × 10−6 5.71 × 10−7 6.74 × 10 −8 87.75 18.29 1.61 × 10−6
MDD cg02280719 1 6 802 222 0.0400 0.0064 5.99 × 10 −10 0.0174 0.0043 5.32 × 10−5
cg08548783 6 57 903 690 0.0378 0.0067 1.37 × 10 −8 0.0142 0.0043 9.79 × 10−4

Note: MWAS 1 results are from a methylome-wide association analysis using linear regression and MWAS 2 results are from a methylome-wide association analysis using OSCA. Bold P-values indicate an association after correction for multiple testing (P < 7.01 × 10−8). Sites are ordered by phenotype and then genomic position. Chromosome number (Chr) and base pair (BP) position are based on genome assembly GRCh37 (hg19). Annotation of genes is provided by missMethyl.