CpG ID
|
β fold change
|
Adjusted p value
|
Chromosome
|
Position (bp)
|
Gene annotation
|
---|
cg11166600
|
0.1002
|
0.0037
|
chr3
|
143,695,141
|
C3orf58 (body)
|
cg15427886
|
0.0896
|
0.0039
|
chr8
|
55,379,663
|
–
|
cg14116799
|
− 0.0764
|
0.0092
|
chr10
|
43,800,154
|
–
|
cg03213396
|
0.0699
|
0.0107
|
chr19
|
53,760,449
|
VN1R2 (TSS1500)
|
cg25024195
|
0.0925
|
0.0253
|
chr17
|
46,144,968
|
–
|
cg03638479
|
− 0.0667
|
0.0253
|
chr3
|
52,009,768
|
ABHD14B (TSS1500);
ABHD14A (body)
|
cg14525247
|
0.0630
|
0.0253
|
chr9
|
131,154,899
|
MIR219–2 (body)
|
cg25275750
|
0.0562
|
0.0410
|
chr13
|
75,918,697
|
TBC1D4 (body)
|
cg10544031
|
− 0.0261
|
0.0410
|
chr2
|
223,164,635
|
PAX3 (TSS1500, 5′UTR);
CCDC140 (TSS1500)
|
cg22871870
|
0.0525
|
0.0415
|
chr15
|
77,348,431
|
TSPAN3 (body)
|
cg20664238
|
0.0193
|
0.0415
|
chr15
|
88,798,877
|
NTRK3 (body)
|
cg05673214
|
0.0498
|
0.0415
|
chr16
|
743,476
|
FBXL16 (3′UTR)
|
cg01215511
|
0.0681
|
0.0414
|
chr16
|
2,975,552
|
FLYWCH1 (5′UTR)
|
cg09288320
|
0.0770
|
0.0415
|
chr2
|
210,994,670
|
C2orf67 (Body)
|
cg00137855
|
0.0612
|
0.0415
|
chr5
|
74,163,723
|
FAM169A (TSS1500)
|
cg19377326
|
0.0657
|
0.0416
|
chr1
|
31,486,063
|
PUM1 (Body)
|
cg03729042
|
0.0444
|
0.0416
|
chr1
|
183,560,923
|
NCF2 (TSS1500)
|
cg00589617
|
0.0647
|
0.0416
|
chr1
|
230,415,343
|
GALNT2 (3’UTR)
|
cg24250902
|
0.0682
|
0.0416
|
chr1
|
230,415,547
|
GALNT2 (3’UTR)
|
cg03754250
|
− 0.0394
|
0.0416
|
chr10
|
31,320,338
|
ZNF438 (5’UTR, Body)
|
- Wave 0 was used as the reference. Annotation was performed according to hg19, and the probe location and gene annotation were taken from Illumina reference files. CpG ID unique identifier from the Illumina CG database. Adjusted p value: false discovery rate (FDR) procedure using the Benjamini–Hochberg method (FDR < 0.05). TSS1500 200–1500 bases upstream of the transcriptional start site (TSS)