108873648:splice
108873648:variant
goto
CCDC138intron_variantc.1832+59A>G
SEPTIN10
Brain_Caudate_basal_ganglia
4.572
0.407
81521217
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(16): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(212): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(214): Hide
0.982
11
11
10
chr2_108873648_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108837653:splice
108837653:variant
goto
CCDC138intron_variantc.1207-1532A>G
CCDC138
Esophagus_Mucosa
5.313
-0.477
81521217
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(16): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(212): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(214): Hide
0.985
18
18
10
chr2_108837653_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108873648:splice
108873648:variant
goto
CCDC138intron_variantc.1832+59A>G
GCC2
Thyroid
3.681
-0.488
81521217
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(16): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(212): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(214): Hide
0.988
17
17
10
chr2_108873648_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108876451:splice
108876451:variant
goto
CCDC1383_prime_UTR_variantc.*198A>G
GCC2
Adipose_Subcutaneous
4.463
0.271
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.927
101
104
10
chr2_108876451_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108878059:splice
108878059:variant
goto
CCDC138downstream_gene_variantc.*1806C>T others(5): Hide
GCC2
Adipose_Subcutaneous
4.689
0.278
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.926
102
105
10
chr2_108878059_C_T_b38
+
MODIFIER
chr2
C
T
TogoVar
108876451:splice
108876451:variant
goto
CCDC1383_prime_UTR_variantc.*198A>G
CCDC138
Brain_Cerebellum
4.022
0.460
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.924
38
40
10
chr2_108876451_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108878059:splice
108878059:variant
goto
CCDC138downstream_gene_variantc.*1806C>T others(5): Hide
CCDC138
Brain_Cerebellum
3.918
0.448
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.922
39
41
10
chr2_108878059_C_T_b38
+
MODIFIER
chr2
C
T
TogoVar
108876451:splice
108876451:variant
goto
CCDC1383_prime_UTR_variantc.*198A>G
CCDC138
Esophagus_Mucosa
3.773
-0.184
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.932
78
83
10
chr2_108876451_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108878059:splice
108878059:variant
goto
CCDC138downstream_gene_variantc.*1806C>T others(5): Hide
CCDC138
Esophagus_Mucosa
3.773
-0.184
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.932
78
83
10
chr2_108878059_C_T_b38
+
MODIFIER
chr2
C
T
TogoVar
108876451:splice
108876451:variant
goto
CCDC1383_prime_UTR_variantc.*198A>G
CCDC138
Heart_Atrial_Appendage
4.129
-0.302
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.916
73
77
10
chr2_108876451_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108878059:splice
108878059:variant
goto
CCDC138downstream_gene_variantc.*1806C>T others(5): Hide
CCDC138
Heart_Atrial_Appendage
4.184
-0.304
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.915
74
78
10
chr2_108878059_C_T_b38
+
MODIFIER
chr2
C
T
TogoVar
108876451:splice
108876451:variant
goto
CCDC1383_prime_UTR_variantc.*198A>G
RANBP2
Nerve_Tibial
4.515
0.188
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.930
89
93
10
chr2_108876451_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108878059:splice
108878059:variant
goto
CCDC138downstream_gene_variantc.*1806C>T others(5): Hide
RANBP2
Nerve_Tibial
4.085
0.177
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.930
90
94
10
chr2_108878059_C_T_b38
+
MODIFIER
chr2
C
T
TogoVar
108876451:splice
108876451:variant
goto
CCDC1383_prime_UTR_variantc.*198A>G
GCC2
Skin_Not_Sun_Exposed_Suprapubic
4.528
0.229
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.929
88
92
10
chr2_108876451_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108878059:splice
108878059:variant
goto
CCDC138downstream_gene_variantc.*1806C>T others(5): Hide
GCC2
Skin_Not_Sun_Exposed_Suprapubic
4.402
0.225
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.928
89
93
10
chr2_108878059_C_T_b38
+
MODIFIER
chr2
C
T
TogoVar
108876451:splice
108876451:variant
goto
CCDC1383_prime_UTR_variantc.*198A>G
GCC2
Skin_Sun_Exposed_Lower_leg
5.912
0.228
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.929
101
106
10
chr2_108876451_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108878059:splice
108878059:variant
goto
CCDC138downstream_gene_variantc.*1806C>T others(5): Hide
GCC2
Skin_Sun_Exposed_Lower_leg
5.850
0.226
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.929
102
107
10
chr2_108878059_C_T_b38
+
MODIFIER
chr2
C
T
TogoVar
108876451:splice
108876451:variant
goto
CCDC1383_prime_UTR_variantc.*198A>G
GCC2
Whole_Blood
4.938
0.169
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.931
105
110
10
chr2_108876451_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108878059:splice
108878059:variant
goto
CCDC138downstream_gene_variantc.*1806C>T others(5): Hide
GCC2
Whole_Blood
5.161
0.172
81519211
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(206): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(208): Hide
0.931
106
111
10
chr2_108878059_C_T_b38
+
MODIFIER
chr2
C
T
TogoVar
108832107:splice
108832107:variant
goto
CCDC138intron_variantc.1207-7078T>G
GCC2
Adipose_Subcutaneous
5.786
0.289
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.911
123
126
10
chr2_108832107_T_G_b38
+
MODIFIER
chr2
T
G
TogoVar
108834460:splice
108834460:variant
goto
CCDC138intron_variantc.1207-4725A>G
GCC2
Adipose_Subcutaneous
5.735
0.281
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.909
126
130
10
chr2_108834460_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108842992:splice
108842992:variant
goto
CCDC138intron_variantc.1323+3691G>A
GCC2
Adipose_Subcutaneous
6.692
0.305
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.908
127
131
10
chr2_108842992_G_A_b38
+
MODIFIER
chr2
G
A
TogoVar
108843542:splice
108843542:variant
goto
CCDC138intron_variantc.1324-3196T>C
GCC2
Adipose_Subcutaneous
5.913
0.289
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.911
123
127
10
chr2_108843542_T_C_b38
+
MODIFIER
chr2
T
C
TogoVar
108845817:splice
108845817:variant
goto
CCDC138intron_variantc.1324-921T>C
GCC2
Adipose_Subcutaneous
5.297
0.269
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.911
122
127
10
chr2_108845817_T_C_b38
+
MODIFIER
chr2
T
C
TogoVar
108846060:splice
108846060:variant
goto
CCDC138intron_variantc.1324-678A>T
GCC2
Adipose_Subcutaneous
4.717
0.249
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.906
128
133
10
chr2_108846060_A_T_b38
+
MODIFIER
chr2
A
T
TogoVar
108856306:splice
108856306:variant
goto
CCDC138intron_variantc.1517-487_1517-486 others(10): Hide
GCC2
Adipose_Subcutaneous
5.238
0.271
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.912
121
125
10
chr2_108856306_C_CTT_b38
+
MODIFIER
chr2
C
CTT
TogoVar
108862398:splice
108862398:variant
goto
CCDC138intron_variantc.1693+5428A>G
GCC2
Adipose_Subcutaneous
5.465
0.277
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.911
122
126
10
chr2_108862398_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108862948:splice
108862948:variant
goto
CCDC138intron_variantc.1693+5985delAothers(1): Hide
GCC2
Adipose_Subcutaneous
5.465
0.277
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.911
122
126
10
chr2_108862948_TA_T_b38
+
MODIFIER
chr2
TA
T
TogoVar
108878843:splice
108878843:variant
goto
CCDC138downstream_gene_variantc.*2590A>G others(5): Hide
GCC2
Adipose_Subcutaneous
5.465
0.277
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.911
122
126
10
chr2_108878843_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108832107:splice
108832107:variant
goto
CCDC138intron_variantc.1207-7078T>G
GCC2
Adipose_Visceral_Omentum
4.340
0.192
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.914
95
100
10
chr2_108832107_T_G_b38
+
MODIFIER
chr2
T
G
TogoVar
108834460:splice
108834460:variant
goto
CCDC138intron_variantc.1207-4725A>G
GCC2
Adipose_Visceral_Omentum
4.227
0.185
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.911
98
104
10
chr2_108834460_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108842992:splice
108842992:variant
goto
CCDC138intron_variantc.1323+3691G>A
GCC2
Adipose_Visceral_Omentum
4.438
0.188
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.909
100
106
10
chr2_108842992_G_A_b38
+
MODIFIER
chr2
G
A
TogoVar
108843542:splice
108843542:variant
goto
CCDC138intron_variantc.1324-3196T>C
GCC2
Adipose_Visceral_Omentum
3.934
0.178
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.912
97
103
10
chr2_108843542_T_C_b38
+
MODIFIER
chr2
T
C
TogoVar
108846060:splice
108846060:variant
goto
CCDC138intron_variantc.1324-678A>T
CCDC138
Brain_Cerebellum
4.473
0.432
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.903
47
51
10
chr2_108846060_A_T_b38
+
MODIFIER
chr2
A
T
TogoVar
108832107:splice
108832107:variant
goto
CCDC138intron_variantc.1207-7078T>G
CCDC138
Cells_Cultured_fibroblasts
3.797
-0.117
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.911
113
116
10
chr2_108832107_T_G_b38
+
MODIFIER
chr2
T
G
TogoVar
108834460:splice
108834460:variant
goto
CCDC138intron_variantc.1207-4725A>G
CCDC138
Cells_Cultured_fibroblasts
3.918
-0.117
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.909
114
118
10
chr2_108834460_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108842992:splice
108842992:variant
goto
CCDC138intron_variantc.1323+3691G>A
CCDC138
Cells_Cultured_fibroblasts
3.674
-0.112
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.908
115
119
10
chr2_108842992_G_A_b38
+
MODIFIER
chr2
G
A
TogoVar
108845817:splice
108845817:variant
goto
CCDC138intron_variantc.1324-921T>C
CCDC138
Cells_Cultured_fibroblasts
3.692
-0.114
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.912
109
114
10
chr2_108845817_T_C_b38
+
MODIFIER
chr2
T
C
TogoVar
108846060:splice
108846060:variant
goto
CCDC138intron_variantc.1324-678A>T
CCDC138
Cells_Cultured_fibroblasts
3.440
-0.108
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.906
118
122
10
chr2_108846060_A_T_b38
+
MODIFIER
chr2
A
T
TogoVar
108856306:splice
108856306:variant
goto
CCDC138intron_variantc.1517-487_1517-486 others(10): Hide
CCDC138
Cells_Cultured_fibroblasts
3.717
-0.116
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.914
108
112
10
chr2_108856306_C_CTT_b38
+
MODIFIER
chr2
C
CTT
TogoVar
108862398:splice
108862398:variant
goto
CCDC138intron_variantc.1693+5428A>G
CCDC138
Cells_Cultured_fibroblasts
3.525
-0.112
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.913
109
113
10
chr2_108862398_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108862948:splice
108862948:variant
goto
CCDC138intron_variantc.1693+5985delAothers(1): Hide
CCDC138
Cells_Cultured_fibroblasts
3.525
-0.112
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.913
109
113
10
chr2_108862948_TA_T_b38
+
MODIFIER
chr2
TA
T
TogoVar
108878843:splice
108878843:variant
goto
CCDC138downstream_gene_variantc.*2590A>G others(5): Hide
CCDC138
Cells_Cultured_fibroblasts
3.525
-0.112
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.913
109
113
10
chr2_108878843_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108832107:splice
108832107:variant
goto
CCDC138intron_variantc.1207-7078T>G
GCC2
Esophagus_Mucosa
3.609
0.206
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
94
99
10
chr2_108832107_T_G_b38
+
MODIFIER
chr2
T
G
TogoVar
108834460:splice
108834460:variant
goto
CCDC138intron_variantc.1207-4725A>G
GCC2
Esophagus_Mucosa
3.825
0.208
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.915
98
104
10
chr2_108834460_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108842992:splice
108842992:variant
goto
CCDC138intron_variantc.1323+3691G>A
GCC2
Esophagus_Mucosa
3.888
0.210
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.916
97
103
10
chr2_108842992_G_A_b38
+
MODIFIER
chr2
G
A
TogoVar
108843542:splice
108843542:variant
goto
CCDC138intron_variantc.1324-3196T>C
GCC2
Esophagus_Mucosa
3.772
0.210
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
99
10
chr2_108843542_T_C_b38
+
MODIFIER
chr2
T
C
TogoVar
108856306:splice
108856306:variant
goto
CCDC138intron_variantc.1517-487_1517-486 others(10): Hide
GCC2
Esophagus_Mucosa
3.772
0.210
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
99
10
chr2_108856306_C_CTT_b38
+
MODIFIER
chr2
C
CTT
TogoVar
108862398:splice
108862398:variant
goto
CCDC138intron_variantc.1693+5428A>G
GCC2
Esophagus_Mucosa
3.772
0.210
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
99
10
chr2_108862398_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108862948:splice
108862948:variant
goto
CCDC138intron_variantc.1693+5985delAothers(1): Hide
GCC2
Esophagus_Mucosa
3.772
0.210
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
99
10
chr2_108862948_TA_T_b38
+
MODIFIER
chr2
TA
T
TogoVar
108878843:splice
108878843:variant
goto
CCDC138downstream_gene_variantc.*2590A>G others(5): Hide
GCC2
Esophagus_Mucosa
3.772
0.210
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
99
10
chr2_108878843_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108832107:splice
108832107:variant
goto
CCDC138intron_variantc.1207-7078T>G
CCDC138
Esophagus_Mucosa
4.016
-0.177
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
94
99
10
chr2_108832107_T_G_b38
+
MODIFIER
chr2
T
G
TogoVar
108834460:splice
108834460:variant
goto
CCDC138intron_variantc.1207-4725A>G
CCDC138
Esophagus_Mucosa
4.419
-0.182
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.915
98
104
10
chr2_108834460_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108842992:splice
108842992:variant
goto
CCDC138intron_variantc.1323+3691G>A
CCDC138
Esophagus_Mucosa
4.904
-0.194
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.916
97
103
10
chr2_108842992_G_A_b38
+
MODIFIER
chr2
G
A
TogoVar
108843542:splice
108843542:variant
goto
CCDC138intron_variantc.1324-3196T>C
CCDC138
Esophagus_Mucosa
4.231
-0.181
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
99
10
chr2_108843542_T_C_b38
+
MODIFIER
chr2
T
C
TogoVar
108845817:splice
108845817:variant
goto
CCDC138intron_variantc.1324-921T>C
CCDC138
Esophagus_Mucosa
3.879
-0.171
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
100
10
chr2_108845817_T_C_b38
+
MODIFIER
chr2
T
C
TogoVar
108846060:splice
108846060:variant
goto
CCDC138intron_variantc.1324-678A>T
CCDC138
Esophagus_Mucosa
3.884
-0.168
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.913
101
107
10
chr2_108846060_A_T_b38
+
MODIFIER
chr2
A
T
TogoVar
108856306:splice
108856306:variant
goto
CCDC138intron_variantc.1517-487_1517-486 others(10): Hide
CCDC138
Esophagus_Mucosa
4.231
-0.181
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
99
10
chr2_108856306_C_CTT_b38
+
MODIFIER
chr2
C
CTT
TogoVar
108862398:splice
108862398:variant
goto
CCDC138intron_variantc.1693+5428A>G
CCDC138
Esophagus_Mucosa
4.231
-0.181
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
99
10
chr2_108862398_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108862948:splice
108862948:variant
goto
CCDC138intron_variantc.1693+5985delAothers(1): Hide
CCDC138
Esophagus_Mucosa
4.231
-0.181
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
99
10
chr2_108862948_TA_T_b38
+
MODIFIER
chr2
TA
T
TogoVar
108878843:splice
108878843:variant
goto
CCDC138downstream_gene_variantc.*2590A>G others(5): Hide
CCDC138
Esophagus_Mucosa
4.231
-0.181
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.919
93
99
10
chr2_108878843_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108832107:splice
108832107:variant
goto
CCDC138intron_variantc.1207-7078T>G
GCC2
Esophagus_Muscularis
3.749
0.149
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.911
94
100
10
chr2_108832107_T_G_b38
+
MODIFIER
chr2
T
G
TogoVar
108834460:splice
108834460:variant
goto
CCDC138intron_variantc.1207-4725A>G
GCC2
Esophagus_Muscularis
4.094
0.155
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.908
97
103
10
chr2_108834460_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108842992:splice
108842992:variant
goto
CCDC138intron_variantc.1323+3691G>A
GCC2
Esophagus_Muscularis
4.156
0.157
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.909
96
102
10
chr2_108842992_G_A_b38
+
MODIFIER
chr2
G
A
TogoVar
108832107:splice
108832107:variant
goto
CCDC138intron_variantc.1207-7078T>G
CCDC138
Heart_Atrial_Appendage
3.965
-0.284
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.907
82
86
10
chr2_108832107_T_G_b38
+
MODIFIER
chr2
T
G
TogoVar
108834460:splice
108834460:variant
goto
CCDC138intron_variantc.1207-4725A>G
CCDC138
Heart_Atrial_Appendage
4.586
-0.300
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.902
85
90
10
chr2_108834460_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108842992:splice
108842992:variant
goto
CCDC138intron_variantc.1323+3691G>A
CCDC138
Heart_Atrial_Appendage
4.366
-0.291
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.900
87
92
10
chr2_108842992_G_A_b38
+
MODIFIER
chr2
G
A
TogoVar
108845817:splice
108845817:variant
goto
CCDC138intron_variantc.1324-921T>C
CCDC138
Heart_Atrial_Appendage
4.042
-0.281
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.903
84
89
10
chr2_108845817_T_C_b38
+
MODIFIER
chr2
T
C
TogoVar
108846060:splice
108846060:variant
goto
CCDC138intron_variantc.1324-678A>T
CCDC138
Heart_Atrial_Appendage
4.211
-0.279
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.897
89
95
10
chr2_108846060_A_T_b38
+
MODIFIER
chr2
A
T
TogoVar
108856306:splice
108856306:variant
goto
CCDC138intron_variantc.1517-487_1517-486 others(10): Hide
CCDC138
Heart_Atrial_Appendage
3.988
-0.280
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.904
83
88
10
chr2_108856306_C_CTT_b38
+
MODIFIER
chr2
C
CTT
TogoVar
108862398:splice
108862398:variant
goto
CCDC138intron_variantc.1693+5428A>G
CCDC138
Heart_Atrial_Appendage
4.042
-0.281
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.903
84
89
10
chr2_108862398_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108862948:splice
108862948:variant
goto
CCDC138intron_variantc.1693+5985delAothers(1): Hide
CCDC138
Heart_Atrial_Appendage
4.042
-0.281
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.903
84
89
10
chr2_108862948_TA_T_b38
+
MODIFIER
chr2
TA
T
TogoVar
108878843:splice
108878843:variant
goto
CCDC138downstream_gene_variantc.*2590A>G others(5): Hide
CCDC138
Heart_Atrial_Appendage
4.042
-0.281
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.903
84
89
10
chr2_108878843_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108842992:splice
108842992:variant
goto
CCDC138intron_variantc.1323+3691G>A
LIMS1
Heart_Left_Ventricle
3.974
0.162
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.904
83
86
10
chr2_108842992_G_A_b38
+
MODIFIER
chr2
G
A
TogoVar
108843542:splice
108843542:variant
goto
CCDC138intron_variantc.1324-3196T>C
LIMS1
Heart_Left_Ventricle
3.979
0.164
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.908
80
83
10
chr2_108843542_T_C_b38
+
MODIFIER
chr2
T
C
TogoVar
108845817:splice
108845817:variant
goto
CCDC138intron_variantc.1324-921T>C
LIMS1
Heart_Left_Ventricle
3.979
0.164
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.908
80
83
10
chr2_108845817_T_C_b38
+
MODIFIER
chr2
T
C
TogoVar
108846060:splice
108846060:variant
goto
CCDC138intron_variantc.1324-678A>T
LIMS1
Heart_Left_Ventricle
3.910
0.157
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.902
84
88
10
chr2_108846060_A_T_b38
+
MODIFIER
chr2
A
T
TogoVar
108862398:splice
108862398:variant
goto
CCDC138intron_variantc.1693+5428A>G
LIMS1
Heart_Left_Ventricle
3.979
0.164
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.908
80
83
10
chr2_108862398_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108862948:splice
108862948:variant
goto
CCDC138intron_variantc.1693+5985delAothers(1): Hide
LIMS1
Heart_Left_Ventricle
3.979
0.164
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.908
80
83
10
chr2_108862948_TA_T_b38
+
MODIFIER
chr2
TA
T
TogoVar
108878843:splice
108878843:variant
goto
CCDC138downstream_gene_variantc.*2590A>G others(5): Hide
LIMS1
Heart_Left_Ventricle
3.979
0.164
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.908
80
83
10
chr2_108878843_A_G_b38
+
MODIFIER
chr2
A
G
TogoVar
108832107:splice
108832107:variant
goto
CCDC138intron_variantc.1207-7078T>G
GCC2
Lung
3.795
0.175
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide
HG00099.hp1 HG00099.hp2 HG00408.hp1 HG00408.hp2 HG00738.hp1 others(201): Hide
0.912
103
106
10
chr2_108832107_T_G_b38
+
MODIFIER
chr2
T
G
TogoVar
108832107:splice
108832107:variant
goto
CCDC138intron_variantc.1207-7078T>G
GCC2
Muscle_Skeletal
3.619
0.123
81519204
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0004 a0001c0005 a0001c0006 a0001c0010 others(10): Hide
a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 a0001c0004t0002 a0001c0005t0001 others(14): Hide
a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0002g0001 others(199): Hide