BTA
|
base position
|
Imputation accuracy
|
Effect
|
–log10(p)
|
Region
|
Gene
|
Annotation
|
---|
1
|
71,227,484
|
0.9745
|
−1.77
|
9.66
|
70,442,929~71,477,578
|
TNK2
|
intron
|
2
|
126,979,882
|
0.9972
|
−1.31
|
11.46
|
126,041,707~127,230,335
|
PIGV (near)
|
downstream
|
2
|
85991577b
|
0.9542
|
1.30
|
8.91
|
85,042,155~86,241,732
|
ANKRD44
|
intron
|
3
|
7,226,390
|
0.9998
|
−1.09
|
9.01
|
6,264,604~7,476,497
|
NOS1AP
|
intron
|
5
|
93,948,357
|
0.9906
|
3.28
|
62.41
|
93,698,481~94,198,670
|
MGST1
|
intron
|
5
|
20284735b
|
0.9692
|
−1.30
|
9.79
|
20,035,379~20,534,779
|
5S_rRNA (near)
|
intergenic
|
6
|
95,497,933
|
0.9996
|
−1.45
|
14.76
|
95,248,213~95,747,954
|
PAQR3 (near)
|
intergenic
|
6
|
32950721b
|
0.4975
|
6.33
|
11.39
|
32,367,171~33,200,834
|
ENSBTAG00000047255
|
intron
|
7
|
57,287,990
|
0.8807
|
−1.66
|
20.11
|
57,038,215~57,538,309
|
KCTD16
|
intron
|
9
|
38,715,137
|
0.9809
|
−1.47
|
8.89
|
38,345,408~38,965,425
|
LAMA4
|
intron
|
11
|
88,771,449
|
0.9876
|
1.16
|
10.43
|
88,521,462~89,021,477
|
ENSBTAG00000047976 (near)
|
intergenic
|
11
|
15323223b
|
0.8962
|
−1.32
|
9.81
|
14,855,568~15,573,444
|
TTC27
|
intron
|
12
|
68,965,758
|
0.9957
|
−1.10
|
8.93
|
68,502,223~69,216,445
|
ENSBTAG00000045195 (near)
|
intergenic
|
14a
|
1,802,265
|
0.9398
|
−6.93
|
240.56
|
1,549,133~2,049,435
|
DGAT1
|
missense
|
14a
|
1,802,266
|
0.9362
|
−6.93
|
240.56
|
1,549,133~2,049,435
|
DGAT1
|
missense
|
14
|
67981742b
|
0.7652
|
1.65
|
8.71
|
67,117,232~68,231,920
|
STK3
|
intron
|
14
|
1321721c
|
0.4442
|
1.46
|
8.82
|
1,087,168~1,583,427
|
ENSBTAG00000046435
|
missense
|
15
|
65,891,100
|
0.9992
|
1.50
|
12.99
|
65,641,131~66,141,839
|
ELF5 (near)
|
intergenic
|
15
|
25044706b
|
0.9908
|
−1.17
|
9.80
|
24,795,472~25,295,470
|
ZBTB16
|
intron
|
16
|
31,496,700
|
0.9501
|
−1.37
|
9.32
|
30,519,873~31,746,789
|
CNST
|
intron
|
17
|
62,543,160
|
0.9898
|
1.14
|
10.49
|
62,224,291~62,793,298
|
TBX5
|
intron
|
18
|
18,970,551
|
0.9442
|
−1.19
|
10.30
|
18,341,203~19,220,732
|
NKD1 (near)
|
intergenic
|
19
|
27,522,927
|
0.8500
|
−1.32
|
10.86
|
26,625,240~27,773,922
|
ASGR1 (near)
|
intergenic
|
20
|
22,609,736
|
0.9813
|
1.53
|
14.23
|
21,664,412~22,859,809
|
MAP3K1 (near)
|
intergenic
|
20
|
44186112b
|
0.9997
|
1.53
|
10.20
|
43,936,468~44,436,133
|
ENSBTAG00000040572 (near)
|
intergenic
|
26
|
20,547,445
|
0.9993
|
−1.76
|
21.46
|
20,299,309~20,797,570
|
COX15
|
intron
|
26
|
42408595b
|
0.9998
|
−1.21
|
10.30
|
41,409,014~42,658,925
|
TACC2
|
intron
|
29
|
23,609,412
|
0.7717
|
2.06
|
10.73
|
22,613,737~23,859,451
|
ENSBTAG00000047094 (near)
|
intergenic
|
Total number of significant SNPs
|
52,334
|
- aFourteen additional SNPs on chromosome 14 located near DGAT1 gene had same highest P value (details on those not presented). Note, bindicated this SNP was found on second round, cindicated this SNP was found on third round