50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
PYGL
Artery_Tibial
7.280
-0.170
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.728
328
375
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
NIN
Colon_Transverse
5.213
0.164
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.700
254
287
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
ABHD12B
Colon_Transverse
9.078
0.332
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.700
254
287
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
PYGL
Colon_Transverse
7.730
0.309
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.700
254
287
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
NIN
Esophagus_Mucosa
32.493
0.453
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.731
297
330
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
ABHD12B
Esophagus_Mucosa
13.038
0.389
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.731
297
330
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
PYGL
Esophagus_Mucosa
32.638
0.443
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.731
297
330
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
PYGL
Skin_Not_Sun_Exposed_Suprapubic
4.800
-0.144
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.720
318
364
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
PYGL
Skin_Sun_Exposed_Lower_leg
6.494
-0.169
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.719
365
422
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50892076:splice
50892076:variant
goto
ABHD12Bintron_variantc.780+3173C>T
ABHD12B
Whole_Blood
4.742
0.108
61126199
a0001 a0002 a0003 a0004 a0006 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(6): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(194): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Hide
0.729
382
434
10
chr14_50892076_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50871519:splice
50871519:variant
goto
ABHD12Bupstream_gene_variantc.-656A>Gothers(2): Hide
ABHD12B
Colon_Transverse
4.922
0.325
81427252
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0002c0002 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0016 a0001c0005t0004 others(22): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0018 others(247): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Hide
0.865
116
129
10
chr14_50871519_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Artery_Tibial
4.327
-0.182
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.128
159
177
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Cells_Cultured_fibroblasts
4.687
0.164
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.126
144
163
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Esophagus_Mucosa
6.164
0.270
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.126
138
155
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Esophagus_Muscularis
6.315
-0.210
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.127
128
143
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
ABHD12B
Nerve_Tibial
5.580
0.342
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.127
152
170
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Stomach
5.650
-0.194
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.144
102
117
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50897112:splice
50897112:variant
goto
ABHD12Bintron_variantc.781-4717A>G
PYGL
Thyroid
4.738
-0.186
61226103
a0001 a0002 a0003 a0004 a0008 others(1): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(21): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 others(98): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00609.hp2 others(103): Hide
0.131
160
179
10
chr14_50897112_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Adipose_Subcutaneous
12.185
0.158
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.325
395
462
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Adipose_Visceral_Omentum
6.477
0.134
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.320
322
374
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Adrenal_Gland
4.746
0.224
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.324
162
191
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Breast_Mammary_Tissue
5.988
0.107
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.322
278
329
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
NIN
Colon_Transverse
5.213
-0.162
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.331
269
316
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
ABHD12B
Colon_Transverse
12.554
-0.387
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.331
269
316
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Colon_Transverse
17.051
-0.455
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.331
269
316
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
NIN
Esophagus_Mucosa
35.494
-0.437
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.318
333
391
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
ABHD12B
Esophagus_Mucosa
18.330
-0.427
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.318
333
391
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Esophagus_Mucosa
32.099
-0.408
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.318
333
391
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Heart_Left_Ventricle
8.605
0.196
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.311
241
280
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Lung
6.171
0.129
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.306
315
368
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Skin_Sun_Exposed_Lower_leg
4.151
0.131
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.320
410
480
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
ABHD12B
Spleen
5.943
-0.271
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.341
159
189
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Spleen
6.144
0.129
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.341
159
189
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
ABHD12B
Whole_Blood
5.042
-0.108
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.314
431
502
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50909079:splice
50909079:variant
goto
ABHD12Bdownstream_gene_variantc.*4713T>G others(5): Hide
PYGL
Whole_Blood
9.706
0.076
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.314
431
502
10
chr14_50909079_T_G_b38
+
MODIFIER
chr14
T
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Adipose_Subcutaneous
8.907
0.145
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.238
306
339
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Adipose_Visceral_Omentum
4.964
0.127
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.232
247
271
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Artery_Tibial
6.895
0.177
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.231
289
319
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Brain_Frontal_Cortex_BA9
4.120
0.196
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.216
101
116
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Breast_Mammary_Tissue
6.402
0.122
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.236
216
241
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
ABHD12B
Cells_Cultured_fibroblasts
5.881
-0.225
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.230
267
298
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
ABHD12B
Colon_Sigmoid
5.295
-0.344
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.215
165
180
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
NIN
Colon_Transverse
11.391
-0.268
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.236
208
226
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
ABHD12B
Colon_Transverse
20.442
-0.536
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.236
208
226
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Colon_Transverse
21.300
-0.554
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.236
208
226
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
NIN
Esophagus_Mucosa
62.791
-0.599
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.234
258
287
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
ABHD12B
Esophagus_Mucosa
35.318
-0.627
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.234
258
287
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Esophagus_Mucosa
65.304
-0.595
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.234
258
287
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
ABHD12B
Liver
5.033
-0.397
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.224
102
117
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Lung
3.931
0.112
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.217
236
261
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
ABHD12B
Nerve_Tibial
7.445
-0.291
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.235
282
314
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
ABHD12B
Pituitary
4.649
-0.278
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.232
125
144
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Skin_Not_Sun_Exposed_Suprapubic
6.877
0.189
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.231
272
300
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Skin_Sun_Exposed_Lower_leg
10.168
0.230
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.239
322
359
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
ABHD12B
Spleen
7.666
-0.350
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.256
131
142
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
NIN
Vagina
6.324
-0.390
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.271
82
92
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
ABHD12B
Vagina
5.452
-0.533
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.271
82
92
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Vagina
5.168
-0.333
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.271
82
92
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
ABHD12B
Whole_Blood
7.509
-0.145
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.228
330
365
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50905615:splice
50905615:variant
goto
ABHD12Bdownstream_gene_variantc.*1249A>G others(5): Hide
PYGL
Whole_Blood
5.729
0.061
5813152
a0001 a0002 a0005 a0009 a0010
a0001c0001 a0001c0006 a0001c0013 a0002c0002 a0002c0004 others(3): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0002c0002t0002 others(8): Hide
a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(147): Hide
HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 HG00438.hp2 others(153): Hide
0.228
330
365
10
chr14_50905615_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Adipose_Subcutaneous
12.017
0.156
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.326
396
463
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Adipose_Visceral_Omentum
6.477
0.134
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.320
322
374
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Adrenal_Gland
4.569
0.219
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.325
163
192
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Breast_Mammary_Tissue
6.160
0.108
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.323
279
330
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
NIN
Colon_Transverse
5.231
-0.162
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
ABHD12B
Colon_Transverse
12.791
-0.391
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Colon_Transverse
17.098
-0.456
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
NIN
Esophagus_Mucosa
36.089
-0.441
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
334
392
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
ABHD12B
Esophagus_Mucosa
18.743
-0.432
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
334
392
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Esophagus_Mucosa
32.848
-0.413
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
334
392
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Heart_Left_Ventricle
8.301
0.193
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.312
242
281
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Lung
6.171
0.129
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.306
315
368
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Skin_Sun_Exposed_Lower_leg
4.151
0.131
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.320
410
480
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
ABHD12B
Spleen
5.943
-0.271
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.341
159
189
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Spleen
6.144
0.129
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.341
159
189
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
ABHD12B
Whole_Blood
5.143
-0.110
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.314
432
503
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50907707:splice
50907707:variant
goto
ABHD12Bdownstream_gene_variantc.*3341A>T others(5): Hide
PYGL
Whole_Blood
9.407
0.074
71330205
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.314
432
503
10
chr14_50907707_A_T_b38
+
MODIFIER
chr14
A
T
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Adipose_Subcutaneous
11.931
0.155
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.326
395
463
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Adipose_Visceral_Omentum
6.439
0.133
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.321
322
375
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Adrenal_Gland
4.626
0.221
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.327
163
193
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Breast_Mammary_Tissue
6.090
0.107
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.322
277
329
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
NIN
Colon_Transverse
5.231
-0.162
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
ABHD12B
Colon_Transverse
12.791
-0.391
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Colon_Transverse
17.098
-0.456
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.332
270
317
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
NIN
Esophagus_Mucosa
36.089
-0.441
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0080 others(200): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Hide
0.319
334
392
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
ABHD12B
Esophagus_Mucosa
18.743
-0.432
71330205
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide