Table 2 Statistically significant mutated non-coding regions

From: Initial genome sequencing and analysis of multiple myeloma

Chr

Start

End

Length (nt)

Mut.

Samples

P-value

q-value

Separation (nt)

Gene

Coding events

1

554350

555310

960

3

3

3.86 × 10−6

0.11

494, 44

AK125248 (intron)

1

82793220

82793300

80

2

2

8.39 × 10−6

0.19

8

TTLL7/LPHN2 (IGR)

1

147333070

147335140

2,070

4

3

2.47 × 10−6

0.09

350, 1, 85

NBPFA (intron)

2

40865560

40865630

70

2

2

4.99 × 10−6

0.14

2

SLC8A1/PKDCC (IGR)

3

149273920

149274010

90

2

2

4.80 × 10−6

0.14

78

ZIC4/AGTR1 (IGR)

3

189142550

189143600

1,050

8

5

5.55 × 10−14

3.9 × 10−8

298, 8, 17, 26, 26, 80, 1

BCL6/LPP (IGR)

3

189440810

189441310

500

3

3

2.64 × 10−6

0.09

1, 291

LPP (intron)

4

7819430

7819530

100

2

2

8.01 × 10−6

0.18

26

AFAP1 (intron)

Missense mutation

4

39875900

39876610

710

3

2

5.88 × 10−6

0.16

109, 412

RHOH (intron)

4

62180540

62181370

830

3

3

1.05 × 10−5

0.22

211, 432

LPHN3 (intron)

4

157902080

157904460

2,380

4

4

6.95 × 10−6

0.17

996, 423, 443

PDGFC (3′ UTR/intron)

7

92754250

92754270

20

2

2

2.03 × 10−7

0.02

1

CCDC132 (intron)

9

16564360

16565100

740

3

2

8.65 × 10−6

0.19

250, 76

BNC2 (intron)

12

120943010

120943460

450

3

3

6.99 × 10−7

0.04

17, 9

BCL7A (promoter)

12

120943580

120946950

3,370

4

3

1.47 × 10−8

0.0017

2055, 657, 295

BCL7A (promoter/intron)

14

68327320

68333190

5,870

4

4

7.05 × 10−6

0.17

397, 156, 35

ZFP36L1 (intron)

Indel

17

8106910

8111850

4,940

4

2

4.85 × 10−6

0.14

1483, 389, 83

PFAS (intron)

Complex rearrangement

20

60328960

60329510

550

2

2

1.42 × 10−6

0.06

120

LAMA5 (intron)

Missense mutation

  1. Regions of predicted regulatory potential showing mutation frequency beyond that expected by chance are shown (q < 0.25). Mut., mutations. ‘Start’ and ‘End’ columns indicate the first and last nucleotide of regions of regulatory potential according to hg18/NCBI36. ‘Separation’ column indicates the number of nucleotides within the regulatory region separating the observed mutations.