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. 2019 Oct 10;43(1):98–105. doi: 10.2337/dc19-0524

Table 3.

DMRs identified by both comb-p and DMRcate*

DMR CpGs comprising the DMR Direction of association Nearby gene(s) Regulatory feature group/gene group/relation to island
comb-p (500 and 1,000 bp window)
 chr 1: 248100345–248100614 cg00785941, cg03748376, cg04028570, cg08260406, cg08944170, cg20434529, cg20507276 OR2L13, CLK3P2 Promoter-associated/first exon: 5′UTR or TSS200/island or north shore
 chr 10: 135342218–135342413 cg10862468, cg25330361 CYP2E1 NA/body/island
DMRcate (500 bp window)chr 1: 248100407–248100614 cg00785941, cg03748376, cg04028570, cg08260406, cg08944170, cg20507276 OR2L13 Promoter-associated/first exon/5′UTR/island
DMRcate (1,000 bp window) cg00321709, cg10862468, cg19469447, cg23400446, cg24530264, cg25330361 CYP2E1 Unclassified/body/island
 chr 10: 135341870–135342620

NA, not applicable. UTR, untranslated region.

*

DMRs were identified from meta-analysis results for individual CpGs, which used results from robust linear regression models that were adjusted for newborn sex, maternal age (in years), maternal BMI (prepregnancy or early pregnancy), maternal education, maternal smoking status during pregnancy (ever vs. never), maternal genetic ancestry (if available) or maternal race/ethnicity, and estimated cord blood cell fractions.