Trait
|
Probe ID
|
Gene
|
Top cis-eQTL
|
Allele Freq
|
P
eQTL
|
P
GWAS
|
P
SMR
|
P
HEIDI
|
nsnp
|
---|
BIP1
|
ILMN_1665280
|
SPCS1
|
rs998909
|
0.420
|
2.1E-39
|
6.8E-07
|
3.4E-06
|
0.15
|
155
|
CAD
|
ILMN_1713380
|
EIF2B2
|
rs175016
|
0.475
|
1.8E-278
|
4.7E-06
|
5.6E-06
|
0.23
|
189
|
ILMN_1712430
|
ATP5G1
|
rs1962412
|
0.281
|
1.3E-44
|
7.4E-07
|
3.0E-06
|
0.27
|
127
|
CD
|
ILMN_1718852
|
PLCL1
|
rs2117339
|
0.486
|
6.7E-30
|
8.0E-07
|
6.0E-06
|
0.14
|
216
|
ILMN_2122952
|
CISD1
|
rs1199098
|
0.214
|
<1.0E-300
|
1.5E-06
|
1.7E-06
|
0.17
|
241
|
ILMN_2122953
|
rs1550773
|
0.212
|
<1.0E-300
|
2.0E-06
|
2.2E-06
|
0.13
|
217
|
COLLEGE
|
ILMN_1723684
|
DARC
|
rs12075
|
0.456
|
4.8E-107
|
3.3E-06
|
5.4E-06
|
0.47
|
110
|
EDUYEARS
|
ILMN_1718023
|
APEH
|
rs3197999
|
0.291
|
1.1E-27
|
5.7E-07
|
5.5E-06
|
0.08
|
88
|
ILMN_2343048
|
ABCB9
|
rs1615350
|
0.248
|
9.1E-43
|
2.0E-06
|
7.2E-06
|
0.75
|
53
|
ILMN_1738369
|
TUFM
|
rs8049439
|
0.405
|
<1.0E-300
|
1.5E-07
|
1.7E-07
|
0.11
|
37
|
HDL
|
ILMN_1684227
|
GPR146
|
rs1997243
|
0.155
|
2.2E-300
|
2.4E-07
|
3.1E-07
|
0.22
|
130
|
IBD
|
ILMN_1697409
|
TNFRSF14
|
rs734999
|
0.483
|
2.1E-90
|
2.3E-07
|
5.4E-07
|
0.98
|
64
|
ILMN_1727709
|
GPBAR1
|
rs2292550
|
0.405
|
8.3E-43
|
6.3E-08
|
4.9E-07
|
0.24
|
109
|
ILMN_1684628
|
ZFP90
|
rs1182968
|
0.219
|
<1.0E-300
|
3.3E-06
|
3.6E-06
|
0.90
|
311
|
LDL
|
ILMN_1718706
|
ERAL1
|
rs901975
|
0.202
|
6.5E-46
|
2.2E-06
|
6.9E-06
|
0.19
|
66
|
UC
|
ILMN_1744713
|
PARK7
|
rs3766606
|
0.173
|
1.1E-53
|
5.7E-08
|
3.0E-07
|
0.09
|
195
|
ILMN_1727709
|
GPBAR1
|
rs2292550
|
0.405
|
8.3E-43
|
1.2E-07
|
8.1E-07
|
0.12
|
109
|
ILMN_1683811
|
TNPO3
|
rs3807306
|
0.496
|
1.4E-150
|
2.3E-06
|
3.3E-06
|
0.69
|
125
|
-
P
eQTL
p value of the top associated cis-eQTL of the probe, P
GWAS GWAS p value of the top cis-eQTL, P
SMR
p value for gene-trait association from the SMR test, P
HEIDI
p value from HEIDI test to indicate whether the gene-trait association is due to a single shared genetic variant (the smaller P
HEIDI the more likely that there are more than one genetic variant)