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Table 5 Significantly AD-associated probes/genes from transcriptome-wide analyses

From: Genome-wide analysis of genetic predisposition to Alzheimer’s disease and related sex disparities

Probe ID

Gene

Top eQTL

Chromosomal region

Position

A1

A1 Freq

P GWAS

P eQTL

b SMR

SESMR

P SMR

P HEIDI

Plan 1—males and females

 ILMN_1754501

C2orf74

rs720201

2p15

61,149,328

C

0.413

6.94E–04

1.34E–164

0.189

0.047

5.54E–05

6.64E–01

 ILMN_2206098

ATG10

rs11741569

5q14.1

82,030,091

G

0.090

9.96E–04

9.69E–27

−0.391

0.097

5.66E–05

8.32E–02

 ILMN_2359800

MS4A6A

rs7108663

11q12.2

60,260,669

C

0.412

2.17E–04

1.41E–48

0.380

0.088

1.59E–05

8.57E–01

 ILMN_2343047

ABCB9

rs641760

12q24.31

123,034,319

T

0.214

2.75E–04

9.79E–17

−0.650

0.162

6.03E–05

1.14E–01

Plan 2—only males

 ILMN_1700307

ZNF815

rs117856560

7p22.1

5,852,503

C

0.048

1.50E–02

8.23E–49

0.389

0.092

2.22E–05

8.80E–02

 ILMN_1731043

TRA2A

rs1046135

7p15.3

23,530,965

T

0.135

1.89E–03

4.32E–115

−0.294

0.067

1.07E–05

2.51E–01

 ILMN_1671603

MED30

rs10111328

8q24.11

117,525,450

T

0.426

3.79E–04

1.67E–20

1.011

0.232

1.30E–05

8.22E–02

 ILMN_1742789

LPXN

rs7928565

11q12.1

58,587,146

C

0.012

2.47E–02

7.17E–86

−0.287

0.056

2.68E–07

6.20E–01

 ILMN_1913678

IRAK3

rs1436849

12q14.3

66,181,338

T

0.416

1.25E–03

6.14E–35

−0.656

0.160

4.11E–05

6.60E–02

 ILMN_1737561

N4BP2L2

rs718444

13q13.1

32,572,915

T

0.375

1.16E–03

1.80E–53

−0.489

0.119

3.96E–05

2.90E–01

 ILMN_1724734

UQCC

rs2425062

20q11.22

35,335,763

G

0.383

2.01E–04

4.58E–13

−1.356

0.321

2.42E–05

7.78E–01

 ILMN_2296950

APOBEC3F

rs11089928

22q13.1

39,133,424

A

0.068

2.42E–03

7.21E–20

−0.724

0.168

1.60E–05

8.31E–02

 ILMN_1806607

SFN a

rs3817604

1p36.11/4p16.3

1,297,549

T

0.120

4.10E–04

5.77E–10

1.179

0.292

5.49E–05

3.92E–01

Plan 3—only females

 ILMN_1806710

ESPN

rs12074379

1p36.31

6,434,683

T

0.040

7.26E–03

8.51E–40

0.421

0.101

3.38E–05

2.84E–01

 ILMN_1696003

GNAI3

rs2301229

1p13.3

109,594,056

T

0.175

4.92E–04

1.45E–211

−0.209

0.045

4.00E–06

1.21E–01

 ILMN_1741881

C9orf72

rs2282240

9p21.2

27,572,636

T

0.264

2.49E–04

1.18E–90

−0.327

0.070

3.27E–06

5.39E–02

 ILMN_1803925

MTMR3

rs41174

22q12.2

30,030,080

T

0.325

8.34E–04

3.03E–76

0.321

0.078

4.21E–05

4.12E–01

  1. Genomic coordinates are based on Human Genome version 38 (hg38)
  2. AD Alzheimer’s disease, eQTL expression quantitative trait loci, A1 effect allele, A1/A1 freq effect allele and its frequency, GWAS genome-wide association study, SMR summary-data-based Mendelian randomization, SE standard error, HEIDI Heterogeneity in Dependent Instruments
  3. aTrans-eQTL