Table 1 Overview of the confirmed rare folate-sensitive fragile sites and their associated CGG-repeats.

From: Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease

Fragile site

Gene

Region

Cohort polymorphism

Reference units

Median units

Minimum units

Maximum units

FRA2A

AFF3

Intronic

95%*

12

16

1

64

99%

4

15

1

43

5′-UTR

12%

8

9

4

47

FRA7A

ZNF713

* 5′-UTR

81%

12

13

5

53

Intronic

92%

21

18

1

53

FRA10A

FRA10AC1

5′-UTR

72%

8

9

5

115

FRA11A

C11orf80

Exonic

48%

8

10

4

62

FRA11B

CBL

5′-UTR

88%

11

13

6

52

FRA12A

DIP2B

5′-UTR

97%

12

14

8

120

FRA16A

XYLT1

Upstream

95%

4

43

1

83

FRAXA

FMR1

5′-UTR

100%

20

28

4

52

FRAXE

AFF2

5′-UTR

77%*

28

30

1

59

 

34%

4

5

5

55

FRAXF

TMEM185A

5′-UTR

61%

10

12

3

55

  1. *In the case of multiple repeats, the repeat indicated as causative of the associated folate sensitive fragile site.