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Table 2 Differentially methylated CpG sites in the cytogenetic subtypes of ALL

From: Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia

DMC signature

DMCsa

Genesb

Genes unique

DMCs unique

Unique DMCs 

Unique DMCs

(number of patients)

  

to subtypec

to subtype

+ DNAm (%)d

-DNAm (%)e

Constitutive (774)

9,406

2,023

NA

NA

NA

NA

T-ALL (101)

58,157

8,245

895

16,841

15,487 (92.0)

1,365 (8.0)

MLL/11q23 (28)

31,403

7,142

300

1,763

1,285 (72.9)

478 (27.1)

dic(9;20) (20)

53,680

9,009

202

2,370

1,561 (65.9)

809 (34.1)

HeH (187)

42,779

7,773

271

3,014

268 (8.9)

2,746 (91.1)

t(1;19)TCF3/PBX1(23)

21,799

5,956

107

1,110

272 (24.5)

838 (75.5)

t(12;21)ETV6/RUNX1(163)

45,589

7,973

156

2,114

1,126 (53.3)

988 (46.7)

t(9;22)BCR/ABL1(19)

23,871

6,047

36

271

140 (51.7)

131 (48.3)

iAMP21 (10)

44,726

8,614

272

2,656

997 (37.5)

1,659 (62.5)

Undefined (105)

39,262

7,059

3

56

8 (14.3)

48 (85.7)

Non-recurrent (100)

42,109

7,434

2

27

14 (51.9)

13 (48.1)

  1. aDifferentially methylated CpG sites (DMCs) with mean Δβ-values >0.20 and false discovery rate-corrected Wilcoxon rank-sum P-values <0.01.
  2. bThe number of gene regions to which the DMCs are annotated.
  3. cGenes with DMCs are considered unique to a subtype if only that subtype had significant DMCs in the gene region.
  4. dHypermethylated DMCs, + DNA methylation (DNAm).
  5. eHypomethylated DMCs, - DNA methylation (DNAm).