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Table 2 GPEA analysis of 1 Mb genomic regions gene sets for the RNAseq UC GRN

From: Urothelial cancer gene regulatory networks inferred from large-scale RNAseq, Bead and Oligo gene expression data

chr

Locus

Start

Size

Edges

p-value

Census

chr5

q31.3

140000001

74

159

3.6673e-222

 

chr17

q21.2

39000001

61

136

7.6570e-204

 

chr17

q21.2

38500001

49

119

1.1284e-194

RARA, SMARCE1

chr6

p22.2

25500001

50

105

1.0881e-163

 

chr6

p22.2/p22.1

26000001

48

98

2.9016e-153

 

chr5

q31.3

140500001

54

103

1.6926e-152

 

chr19

q13.43

57500001

41

90

3.9091e-150

 

chr8

q24.3

145000001

43

81

1.5314e-127

RECQL4

chr19

q13.43

58000001

46

75

8.4630e-111

 

chr16

p11.2

30000001

54

80

4.0300e-109

 

chr21

q22.11

31500001

38

67

5.2390e-107

 

chr1

q21.3

152500001

43

69

2.0553e-103

 

chr9

q34.3

139500001

67

83

7.6570e-99

 

chr17

q25.3

79500001

47

67

3.9091e-94

ASPSCR1

chr19

q13.31

44000001

37

60

4.0300e-94

 

chr16

p11.2

30500001

49

68

1.7329e-93

FUS

chr8

q24.3

145500001

37

58

4.8360e-90

RECQL4

chr11

q13.1/q13.2

65000001

46

64

8.8660e-90

 

chr3

p25.3

9500001

34

55

3.1837e-88

FANCD2, VHL

chr5

q31.3

139500001

42

60

3.1434e-87

 

chr6

p22.1

27000001

32

51

8.8660e-83

HIST1H4I

chr1

q21.3

152000001

34

52

5.2390e-82

 

chr16

p11.2

29500001

45

59

1.1687e-81

 

chrX

p11.23

48500001

50

62

1.8941e-81

GATA1, TFE3, WAS

chr6

p21.33/p21.32

31500001

79

78

1.2896e-79

 

chr19

p13.3

500001

51

60

7.6570e-77

FSTL3, STK11

chr1

p36.33

1000001

48

58

1.7732e-76

 

chr19

p13.3

1000001

43

54

1.1687e-74

STK11, TCF3

chr1

q21.3

150500001

35

48

1.5314e-72

MLLT11, ARNT

chr1

q22

155000001

42

51

3.3852e-70

MUC1

chr8

q24.3

144500001

39

49

9.2690e-70

 

chr19

q13.41/q13.42

53000001

31

44

1.6926e-69

 

chr19

p13.11/p12

19000001

33

45

5.2390e-69

 

chr16

p13.3

1

52

56

5.6420e-69

AXIN1

chrX

p11.23/p11.22

49000001

44

51

4.4330e-68

 

chr11

q13.1/q13.2

65500001

46

52

7.6570e-68

 

chr6

p22.1

27500001

36

46

2.1359e-67

 

chr19

q13.33

49500001

70

64

2.9822e-66

 

chr1

q23.3

161000001

36

45

1.8941e-65

FCGR2B, SDHC

chr19

q13.31/q13.32

44500001

36

45

1.8941e-65

CBLC, BCL3

chr3

p21.31

48500001

42

48

1.1284e-64

NCKIPSD

chr19

q13.43

58500001

30

41

1.4911e-64

 

chr16

p13.3

1500001

59

57

2.1762e-64

TSC2, TRAF7

chr1

q21.3

151000001

37

45

2.4583e-64

MLLT11

chr11

p15.5

1

50

52

5.2390e-64

HRAS

chr1

q21.3/q22

154500001

42

47

7.6570e-63

MUC1

chr19

q13.12

36000001

48

50

1.9747e-62

 

chr11

q13.1

64500001

56

54

4.4330e-62

MEN1

chr19

p13.2

11500001

30

39

1.9747e-60

 

chr11

q13.2

67000001

36

42

1.1284e-59

 
  1. For each significant genomic region the chromosome (chr), chromosome band (locus), nucleotide base start site of the genomic region (start), number of genes of the gene set (size), number of edges of the significant subnetwork (edges), Bonferroni adjusted p-value of the subnetwork (p-value) and a list of genes in the significant subnetwork that are present in the cancer census (census).