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Table 1 Proportions of the different genotypes associated with nc886 RNA levels, proportions of the nc886 methylation status groups and the proportions of the combinations of these in the cohorts utilised in the study

From: Regulation of nc886 (vtRNA2-1) RNAs is associated with cardiometabolic risk factors and diseases

 

YFS 2007; n = 1497; 30–45 y

DILGOM; n = 504; 25–74 y

LURIC; n = 2183; 17–92 y

KORA F4; n = 1653; 32–81 y

KORA FF4; n = 1771; 38–87 y

Bogalusa; n = 658; 36–57 y

NFBC1966; n = 792; 43–47 y

nc886 methylation

Imprinted

73.20%

72.20%

72.00%

76.50%

75.10%

71.60%

71.80%

Intermethylated

3.20%

6.30%

4.10%

2.60%

3.10%

3.40%

3.20%

Nonmethylated

23.60%

21.40%

23.90%

20.90%

21.70%

24.80%

25.00%

Genotype

T/T

81.60%

85.40%

85.10%

86.80%

86.50%

85.40%

83.10%

T/C

17.40%

14.00%

14.50%

12.70%

12.70%

14.00%

16.10%

C/C

1.00%

0.40%

0.40%

0.50%

0.70%

0.40%

0.80%

Proxy group

Imprinted T/T

59.90%

57.90%

61.30%

66.20%

64.90%

60.90%

59.50%

59,50%

Intermethylated T/T

2.80%

5.90%

3.60%

2.20%

2.60%

2.70%

2.80%

2,80%

Nonmethylated T/T

18.90%

18.40%

20.20%

18.40%

19.00%

21.80%

20.80%

20,80%

Imprinted T/C

12.60%

13.70%

10.40%

9.90%

9.70%

10.30%

12.00%

12,00%

Intermethylated T/C

0.40%

0.40%

0.50%

0.40%

0.50%

0.70%

0.40%

0,40%

Nonmethylated T/C

4.40%

3.00%

3.60%

2.40%

2.50%

3.00%

3.60%

3,60%

Imprinted C/C

0.70%

0.60%

0.30%

0.40%

0.50%

0.40%

0.30%

0,30%

Intermethylated C/C

0%

0%

0%

0%

0%

0%

0%

0%

Nonmethylated C/C

0.30%

0.00%

0.10%

0.10%

0.20%

0.00%

0.60%

0,60%

Use in proxy

Control

59.90%

57.90%

61.30%

66.20%

64.90%

60.90%

59.50%

Elevated nc886 RNA

24.30%

22.00%

24.20%

21.30%

22.20%

25.20%

25.30%

Excluded

15.80%

20.00%

14.50%

12.50%

12.80%

13.70%

15.20%

  1. “Use in proxy” refers to analyses associating the predicted nc886 RNA levels with CMD phenotypes. Intermediately methylated (intermethylated) groups were excluded due to low numbers, and the “Imprinted T/C” group was excluded due to the different effects of a maternally or paternally inherited minor allele, as described in the main body of the text. The total numbers of individuals with available methylation and genotype data, as well as the age ranges, are listed under the cohort names. Other cohort demographics are found in Supplementary Table 1