9101298:splice
9101298:variant
goto
A2Mintron_variantc.1495-91G>A
KLRG1
Adipose_Visceral_Omentum
6.234
0.402
152527251
a0001 a0002 a0003 a0004 a0006 others(10): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0011 others(20): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(22): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0020 others(246): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(297): Hide
0.943
65
66
10
chr12_9101298_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9101298:splice
9101298:variant
goto
A2Mintron_variantc.1495-91G>A
PHC1
Cells_Cultured_fibroblasts
3.747
-0.177
152527251
a0001 a0002 a0003 a0004 a0006 others(10): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0011 others(20): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(22): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0020 others(246): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(297): Hide
0.947
66
69
10
chr12_9101298_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9101298:splice
9101298:variant
goto
A2Mintron_variantc.1495-91G>A
KLRG1
Nerve_Tibial
6.799
0.372
152527251
a0001 a0002 a0003 a0004 a0006 others(10): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0011 others(20): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(22): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0020 others(246): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(297): Hide
0.945
70
73
10
chr12_9101298_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9101298:splice
9101298:variant
goto
A2Mintron_variantc.1495-91G>A
PHC1
Thyroid
4.261
-0.187
152527251
a0001 a0002 a0003 a0004 a0006 others(10): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0011 others(20): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(22): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0020 others(246): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(297): Hide
0.941
79
81
10
chr12_9101298_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
KLRG1
Adipose_Subcutaneous
4.353
0.168
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.842
204
225
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
A2M
Adipose_Subcutaneous
11.112
-0.256
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.842
204
225
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
KLRG1
Adipose_Visceral_Omentum
5.890
0.244
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.840
172
187
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
M6PR
Artery_Aorta
4.743
0.118
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.852
131
140
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
M6PR
Artery_Tibial
6.434
0.177
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.843
201
217
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
KLRG1
Brain_Nucleus_accumbens_basal_ganglia
4.292
0.297
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.842
77
90
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
KLRG1
Breast_Mammary_Tissue
5.784
0.217
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.839
148
165
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
M6PR
Cells_Cultured_fibroblasts
9.745
0.168
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.838
192
210
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
KLRG1
Cells_Cultured_fibroblasts
8.301
0.331
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.838
192
210
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
A2M
Cells_Cultured_fibroblasts
3.977
-0.140
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.838
192
210
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
M6PR
Lung
4.211
0.086
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.835
178
198
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
KLRG1
Muscle_Skeletal
3.765
0.156
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.849
227
246
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
A2M
Muscle_Skeletal
5.127
-0.131
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.849
227
246
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
KLRG1
Nerve_Tibial
4.238
0.179
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.843
188
209
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
M6PR
Skin_Not_Sun_Exposed_Suprapubic
8.092
0.177
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.836
194
213
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
M6PR
Skin_Sun_Exposed_Lower_leg
5.021
0.139
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.847
209
230
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
A2M
Skin_Sun_Exposed_Lower_leg
4.695
-0.104
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.847
209
230
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9110635:splice
9110635:variant
goto
A2Mintron_variantc.484-301T>C
KLRG1
Thyroid
3.857
0.157
111921208
a0001 a0002 a0003 a0004 a0009 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0003t0002 a0001c0005t0002 a0001c0009t0002 others(16): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(203): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Hide
0.836
203
223
10
chr12_9110635_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Adipose_Subcutaneous
17.143
0.268
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.344
403
489
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Adipose_Subcutaneous
15.432
0.235
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.344
403
489
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Adipose_Visceral_Omentum
13.875
0.294
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.334
321
390
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Adipose_Visceral_Omentum
4.803
0.134
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.334
321
390
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Adrenal_Gland
8.468
0.353
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.383
181
226
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Artery_Aorta
6.924
0.265
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.329
255
311
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Artery_Tibial
11.960
0.251
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.331
379
456
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Artery_Tibial
6.343
0.135
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.331
379
456
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Brain_Amygdala
6.883
0.401
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.331
97
119
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Brain_Anterior_cingulate_cortex_BA24
14.093
0.493
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.324
125
151
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Brain_Caudate_basal_ganglia
8.058
0.311
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.339
160
202
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Brain_Cerebellar_Hemisphere
18.541
0.407
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.332
147
183
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
PHC1
Brain_Cerebellum
5.617
-0.190
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.318
138
168
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
M6PR
Brain_Cerebellum
6.364
-0.163
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.318
138
168
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Brain_Cerebellum
14.703
0.443
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.318
138
168
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Brain_Cortex
16.399
0.499
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.317
140
170
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Brain_Frontal_Cortex_BA9
13.577
0.429
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.323
141
173
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Brain_Hippocampus
7.608
0.359
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.333
138
169
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Brain_Hypothalamus
13.281
0.376
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.352
141
180
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Brain_Nucleus_accumbens_basal_ganglia
13.329
0.419
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.326
149
185
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Breast_Mammary_Tissue
14.187
0.283
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.333
285
340
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Breast_Mammary_Tissue
5.494
0.123
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.333
285
340
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
M6PR
Cells_Cultured_fibroblasts
4.064
0.083
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.326
355
423
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Cells_Cultured_fibroblasts
29.112
0.490
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.326
355
423
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Cells_Cultured_fibroblasts
8.101
0.164
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.326
355
423
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Cells_EBV-transformed_lymphocytes
5.803
0.300
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.307
173
200
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Colon_Sigmoid
10.377
0.282
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.328
227
274
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Colon_Transverse
5.625
0.127
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.325
260
311
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Esophagus_Gastroesophageal_Junction
5.744
0.205
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.331
224
267
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Esophagus_Gastroesophageal_Junction
10.997
0.308
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.331
224
267
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
PHC1
Esophagus_Mucosa
9.829
-0.193
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.340
345
417
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Esophagus_Mucosa
8.466
0.162
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.340
345
417
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Esophagus_Muscularis
15.265
0.265
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.333
310
374
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Esophagus_Muscularis
13.251
0.250
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.333
310
374
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Heart_Atrial_Appendage
10.589
0.317
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.312
236
287
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Heart_Left_Ventricle
5.703
0.197
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.329
247
296
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Muscle_Skeletal
21.317
0.296
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.337
451
550
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Muscle_Skeletal
6.908
0.117
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.337
451
550
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
CLEC4A
Nerve_Tibial
4.087
-0.129
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.334
364
445
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Nerve_Tibial
10.373
0.226
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.334
364
445
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Nerve_Tibial
11.398
0.172
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.334
364
445
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Pancreas
5.060
0.313
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.331
201
240
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Pituitary
6.174
0.277
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.334
169
208
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Skin_Not_Sun_Exposed_Suprapubic
6.977
0.104
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.344
365
446
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Skin_Sun_Exposed_Lower_leg
5.726
0.166
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.343
420
515
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Skin_Sun_Exposed_Lower_leg
15.215
0.146
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.343
420
515
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Stomach
9.286
0.194
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.354
232
288
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Testis
5.856
0.270
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.317
219
262
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Testis
8.707
0.158
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.317
219
262
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Thyroid
3.953
0.125
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.335
378
456
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
A2M
Thyroid
5.425
0.130
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.335
378
456
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
M6PR
Whole_Blood
4.929
-0.076
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.333
438
533
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
KLRG1
Whole_Blood
9.485
-0.112
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.333
438
533
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9106957:splice
9106957:variant
goto
A2Mintron_variantc.880-352G>A
PZP
Whole_Blood
11.682
-0.205
67784
a0001 a0002 a0003 a0004 a0010 others(1): Hide
a0001c0001 a0001c0026 a0002c0002 a0003c0004 a0004c0006 others(2): Hide
a0001c0001t0001 a0001c0026t0001 a0002c0002t0002 a0003c0004t0001 a0004c0006t0001 others(2): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Hide
HG00099.hp2 HG00140.hp2 HG00408.hp1 HG00544.hp1 HG00558.hp2 others(101): Hide
0.333
438
533
10
chr12_9106957_C_T_b38
-
MODIFIER
chr12
C
T
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
A2M
Adipose_Subcutaneous
8.889
-0.232
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.843
205
223
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
KLRG1
Adipose_Visceral_Omentum
4.996
0.227
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.842
172
185
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
M6PR
Artery_Aorta
4.618
0.118
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.855
129
137
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
M6PR
Artery_Tibial
8.055
0.201
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.844
201
215
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
KLRG1
Brain_Nucleus_accumbens_basal_ganglia
5.067
0.330
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.838
80
92
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
KLRG1
Breast_Mammary_Tissue
6.315
0.234
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.842
147
161
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
A2M
Breast_Mammary_Tissue
5.422
-0.153
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.842
147
161
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
M6PR
Cells_Cultured_fibroblasts
11.998
0.190
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.839
193
209
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
KLRG1
Cells_Cultured_fibroblasts
8.007
0.328
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.839
193
209
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
PHC1
Esophagus_Mucosa
4.033
-0.156
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.847
176
188
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
M6PR
Lung
4.480
0.090
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.834
182
199
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
KLRG1
Muscle_Skeletal
3.903
0.161
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.851
226
243
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
KLRG1
Nerve_Tibial
5.160
0.203
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.846
187
205
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
M6PR
Skin_Not_Sun_Exposed_Suprapubic
8.306
0.182
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.839
193
209
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
M6PR
Skin_Sun_Exposed_Lower_leg
6.055
0.157
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.852
204
222
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
A2M
Skin_Sun_Exposed_Lower_leg
5.396
-0.114
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.852
204
222
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9070851:splice
9070851:variant
goto
A2Mintron_variantc.4104-273T>C
KLRG1
Thyroid
4.496
0.174
111922199
a0001 a0002 a0003 a0004 a0010 others(6): Hide
a0001c0001 a0001c0003 a0001c0005 a0001c0009 a0001c0015 others(14): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 a0001c0003t0002 a0001c0005t0002 others(17): Hide
a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Hide
0.838
204
221
10
chr12_9070851_A_G_b38
-
MODIFIER
chr12
A
G
TogoVar
9074365:splice
9074365:variant
goto
A2Mintron_variantc.3756+195C>T
A2M
Adipose_Subcutaneous
12.486
-0.205
7101290
a0001 a0002 a0009 a0010 a0011 others(2): Hide
a0001c0001 a0001c0005 a0001c0022 a0002c0002 a0002c0010 others(5): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0005t0002 a0001c0022t0002 a0002c0002t0001 others(7): Hide
a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0158 a0001c0001t0001g0170 others(85): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00423.hp2 others(103): Hide
0.496
534
706
10
chr12_9074365_G_A_b38
-
MODIFIER
chr12
G
A
TogoVar
9074365:splice
9074365:variant
goto
A2Mintron_variantc.3756+195C>T
A2M
Adipose_Visceral_Omentum
4.709
-0.124
7101290
a0001 a0002 a0009 a0010 a0011 others(2): Hide
a0001c0001 a0001c0005 a0001c0022 a0002c0002 a0002c0010 others(5): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0005t0002 a0001c0022t0002 a0002c0002t0001 others(7): Hide
a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0158 a0001c0001t0001g0170 others(85): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00423.hp2 others(103): Hide
0.500
436
584
10
chr12_9074365_G_A_b38
-
MODIFIER
chr12
G
A
TogoVar
9074365:splice
9074365:variant
goto
A2Mintron_variantc.3756+195C>T
M6PR
Artery_Tibial
4.518
0.105
7101290
a0001 a0002 a0009 a0010 a0011 others(2): Hide
a0001c0001 a0001c0005 a0001c0022 a0002c0002 a0002c0010 others(5): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0005t0002 a0001c0022t0002 a0002c0002t0001 others(7): Hide
a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0158 a0001c0001t0001g0170 others(85): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00423.hp2 others(103): Hide
0.504
513
684
10
chr12_9074365_G_A_b38
-
MODIFIER
chr12
G
A
TogoVar
9074365:splice
9074365:variant
goto
A2Mintron_variantc.3756+195C>T
NECAP1
Brain_Spinal_cord_cervical_c-1
5.239
0.167
7101290
a0001 a0002 a0009 a0010 a0011 others(2): Hide
a0001c0001 a0001c0005 a0001c0022 a0002c0002 a0002c0010 others(5): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0005t0002 a0001c0022t0002 a0002c0002t0001 others(7): Hide
a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0158 a0001c0001t0001g0170 others(85): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00423.hp2 others(103): Hide
0.517
151
196
10
chr12_9074365_G_A_b38
-
MODIFIER
chr12
G
A
TogoVar
9074365:splice
9074365:variant
goto
A2Mintron_variantc.3756+195C>T
A2M
Breast_Mammary_Tissue
6.574
-0.125
7101290
a0001 a0002 a0009 a0010 a0011 others(2): Hide
a0001c0001 a0001c0005 a0001c0022 a0002c0002 a0002c0010 others(5): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0005t0002 a0001c0022t0002 a0002c0002t0001 others(7): Hide
a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0158 a0001c0001t0001g0170 others(85): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00423.hp2 others(103): Hide
0.508
377
503
10
chr12_9074365_G_A_b38
-
MODIFIER
chr12
G
A
TogoVar
9074365:splice
9074365:variant
goto
A2Mintron_variantc.3756+195C>T
M6PR
Cells_Cultured_fibroblasts
5.212
0.087
7101290
a0001 a0002 a0009 a0010 a0011 others(2): Hide
a0001c0001 a0001c0005 a0001c0022 a0002c0002 a0002c0010 others(5): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0005t0002 a0001c0022t0002 a0002c0002t0001 others(7): Hide
a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0158 a0001c0001t0001g0170 others(85): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00423.hp2 others(103): Hide
0.501
486
648
10
chr12_9074365_G_A_b38
-
MODIFIER
chr12
G
A
TogoVar
9074365:splice
9074365:variant
goto
A2Mintron_variantc.3756+195C>T
A2M
Cells_Cultured_fibroblasts
14.528
-0.203
7101290
a0001 a0002 a0009 a0010 a0011 others(2): Hide
a0001c0001 a0001c0005 a0001c0022 a0002c0002 a0002c0010 others(5): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0005t0002 a0001c0022t0002 a0002c0002t0001 others(7): Hide
a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0158 a0001c0001t0001g0170 others(85): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00423.hp2 others(103): Hide
0.501
486
648
10
chr12_9074365_G_A_b38
-
MODIFIER
chr12
G
A
TogoVar