TABLE 3.
CpG site | Estimate | SE | p | p Bonferroni | CHR | BP | UCSC Ref Gene | Associated variant |
---|---|---|---|---|---|---|---|---|
cg20614157 | 9.04E−04 | 0.0003 | <0.001 | 0.037 | 6 | 31980845 | TNXB,TNXA,STK19 | rs17421133, rs2077116, rs17207951, rs2857009, rs2071295, rs17201588, rs6902493, rs41268896 |
cg19376858 | 8.38E−04 | 0.0003 | 0.008 | 0.084 | 6 | 31980856 | TNXB,TNXA,STK19 |
rs6449, rs3020644, rs9267806, rs4713506, rs6941112, rs4713505, rs9267803, rs6463, rs9267802, rs4151657, rs8111, rs17421133, rs2280774, rs6415128, rs2894250, rs2228628, rs2857009, rs2077116, rs6902493, rs17201588 |
cg15321244 | −2.23E−02 | 0.0088 | 0.011 | 1 | 6 | 32729643 | HLA‐DQB2 | rs9275987, rs2261566 |
cg23928032 | −9.75E−03 | 0.0038 | 0.011 | 1 | 6 | 31964391 | C4B.C4A |
rs9267806, rs4713506, rs4713505, rs9267803, rs6463, rs9267802, rs8111, rs17421133, rs2228628, rs2857009, rs2077116, rs6902493, rs17201588, rs17207951, rs2239689, rs28361052, rs2071295, rs17421624, rs41268896, rs2071293 |
cg01937212 | −1.43E−02 | 0.0062 | 0.020 | 1 | 6 | 32295097 | C6orf10 |
rs9268301, rs9368714, rs2076540, rs2746115, rs2143466, rs761187, rs9268129, rs471081, rs6929776, rs9348880, rs2022533, rs6457544, rs6457543, rs565571, rs9366793, rs9394087, rs9268141, rs546857, rs477005, rs557539 |
cg11391305 | −1.43E−02 | 0.007 | 0.042 | 1 | 6 | 32731438 | HLA‐DQB2 | rs9275987 |
Abbreviations: BP = Genomic position (b37);CHR = chromosome; mQTL = methylation quantitative trait loci; SATSA = Swedish Adoption/Twin Study of Aging; SE = standard error.
If >20 associated variants, the first 20 with lowest p‐values are included (see Table S9 for full results).