50872157:splice
50872157:variant
goto
ABHD12B5_prime_UTR_variantc.-18A>C
VCPKMT
Muscle_Skeletal
3.660
0.377
91526329
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0002c0002 others(10): Hide
a0001c0001t0001 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(21): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(324): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Hide
0.971
41
48
10
chr14_50872157_A_C_b38
+
MODIFIER
chr14
A
C
TogoVar
50884303:splice
50884303:variant
goto
ABHD12Bintron_variantc.487-1311T>C
TMX1
Vagina
5.122
-0.952
91635338
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(30): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(333): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Hide
0.988
3
4
10
chr14_50884303_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50883951:splice
50883951:variant
goto
ABHD12Bintron_variantc.487-1661_487-1660 others(10): Hide
TMX1
Vagina
5.122
-0.952
91635337
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(30): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(332): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Hide
0.988
3
4
10
chr14_50883951_C_CTA_b38
+
MODIFIER
chr14
C
CTA
TogoVar
50884228:splice
50884228:variant
goto
ABHD12Bintron_variantc.487-1386A>G
TMX1
Vagina
5.122
-0.952
91635337
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(30): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(332): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Hide
0.988
3
4
10
chr14_50884228_A_G_b38
+
MODIFIER
chr14
A
G
TogoVar
50884471:splice
50884471:variant
goto
ABHD12Bintron_variantc.487-1143C>G
TMX1
Vagina
5.122
-0.952
91635337
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(30): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(332): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Hide
0.988
3
4
10
chr14_50884471_C_G_b38
+
MODIFIER
chr14
C
G
TogoVar
50884575:splice
50884575:variant
goto
ABHD12Bintron_variantc.487-1039C>T
TMX1
Vagina
5.122
-0.952
91635337
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(30): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(332): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Hide
0.988
3
4
10
chr14_50884575_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50884032:splice
50884032:variant
goto
ABHD12Bintron_variantc.487-1577_487-1575 others(11): Hide
TMX1
Vagina
5.654
-0.808
81429302
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0013 a0002c0002 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(24): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(297): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Hide
0.979
6
7
10
chr14_50884032_GTCA_G_b38
+
MODIFIER
chr14
GTCA
G
TogoVar
50884333:splice
50884333:variant
goto
ABHD12Bintron_variantc.487-1281C>T
TMX1
Vagina
4.903
-0.877
91634331
a0001 a0002 a0003 a0004 a0005 others(4): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(11): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 a0001c0001t0016 a0001c0005t0004 others(29): Hide
a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(326): Hide
HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Hide
0.985
4
5
10
chr14_50884333_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
50869179:splice
50869179:variant
goto
ABHD12Bupstream_gene_variantc.-2996C>A others(3): Hide
ABHD12B
Thyroid
5.388
-0.240
81418130
a0001 a0002 a0003 a0004 a0005 others(3): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(9): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(13): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(125): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(133): Hide
0.385
428
524
10
chr14_50869179_C_A_b38
+
MODIFIER
chr14
C
A
TogoVar
50869019:splice
50869019:variant
goto
ABHD12Bupstream_gene_variantc.-3156T>C others(3): Hide
VCPKMT
Skin_Not_Sun_Exposed_Suprapubic
4.150
0.092
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.371
392
482
10
chr14_50869019_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50869025:splice
50869025:variant
goto
ABHD12Bupstream_gene_variantc.-3150G>A others(3): Hide
VCPKMT
Skin_Not_Sun_Exposed_Suprapubic
4.150
0.092
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.371
392
482
10
chr14_50869025_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50869019:splice
50869019:variant
goto
ABHD12Bupstream_gene_variantc.-3156T>C others(3): Hide
NIN
Thyroid
3.960
-0.102
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.375
418
511
10
chr14_50869019_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50869025:splice
50869025:variant
goto
ABHD12Bupstream_gene_variantc.-3150G>A others(3): Hide
NIN
Thyroid
3.759
-0.100
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.374
418
510
10
chr14_50869025_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50869019:splice
50869019:variant
goto
ABHD12Bupstream_gene_variantc.-3156T>C others(3): Hide
ABHD12B
Thyroid
6.107
-0.259
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.375
418
511
10
chr14_50869019_T_C_b38
+
MODIFIER
chr14
T
C
TogoVar
50869025:splice
50869025:variant
goto
ABHD12Bupstream_gene_variantc.-3150G>A others(3): Hide
ABHD12B
Thyroid
6.056
-0.258
71215126
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(7): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0005t0004 a0001c0005t0007 a0001c0006t0001 others(10): Hide
a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0043 others(121): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Hide
0.374
418
510
10
chr14_50869025_G_A_b38
+
MODIFIER
chr14
G
A
TogoVar
50874372:splice
50874372:variant
goto
ABHD12Bintron_variantc.104+2094G>A
ABHD12B
Thyroid
3.915
-0.228
7101278
a0001 a0002 a0003 a0004 a0005 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0002c0002 a0002c0004 others(5): Hide
a0001c0001t0001 a0001c0005t0004 a0001c0006t0001 a0002c0002t0002 a0002c0002t0005 others(7): Hide
a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0233 others(73): Hide
HG00140.hp1 HG00280.hp1 HG00280.hp2 HG00423.hp1 HG00423.hp2 others(77): Hide
0.239
283
326
10
chr14_50874372_G_A_b38
+
MODIFIER
chr14
G
A
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
50900610:splice
50900610:variant
goto
ABHD12Bintron_variantc.781-1219C>T
PYGL
Artery_Tibial
4.550
-0.211
361164
a0001 a0004 a0008
a0001c0001 a0001c0006 a0001c0013 a0004c0007 a0004c0009 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0004c0007t0001 others(6): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0046 others(59): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Hide
0.084
107
116
10
chr14_50900610_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50900610:splice
50900610:variant
goto
ABHD12Bintron_variantc.781-1219C>T
PYGL
Cells_Cultured_fibroblasts
4.170
0.174
361164
a0001 a0004 a0008
a0001c0001 a0001c0006 a0001c0013 a0004c0007 a0004c0009 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0004c0007t0001 others(6): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0046 others(59): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Hide
0.086
102
111
10
chr14_50900610_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50900610:splice
50900610:variant
goto
ABHD12Bintron_variantc.781-1219C>T
PYGL
Esophagus_Gastroesophageal_Junction
4.234
-0.219
361164
a0001 a0004 a0008
a0001c0001 a0001c0006 a0001c0013 a0004c0007 a0004c0009 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0004c0007t0001 others(6): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0046 others(59): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Hide
0.078
57
63
10
chr14_50900610_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50900610:splice
50900610:variant
goto
ABHD12Bintron_variantc.781-1219C>T
PYGL
Esophagus_Muscularis
3.980
-0.185
361164
a0001 a0004 a0008
a0001c0001 a0001c0006 a0001c0013 a0004c0007 a0004c0009 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0004c0007t0001 others(6): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0046 others(59): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Hide
0.081
86
91
10
chr14_50900610_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50900610:splice
50900610:variant
goto
ABHD12Bintron_variantc.781-1219C>T
PYGL
Pancreas
5.337
-0.339
361164
a0001 a0004 a0008
a0001c0001 a0001c0006 a0001c0013 a0004c0007 a0004c0009 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0004c0007t0001 others(6): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0046 others(59): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Hide
0.093
60
67
10
chr14_50900610_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50900610:splice
50900610:variant
goto
ABHD12Bintron_variantc.781-1219C>T
ABHD12B
Skin_Not_Sun_Exposed_Suprapubic
3.923
-0.142
361164
a0001 a0004 a0008
a0001c0001 a0001c0006 a0001c0013 a0004c0007 a0004c0009 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0004c0007t0001 others(6): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0046 others(59): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Hide
0.082
102
107
10
chr14_50900610_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50900610:splice
50900610:variant
goto
ABHD12Bintron_variantc.781-1219C>T
PYGL
Skin_Not_Sun_Exposed_Suprapubic
5.997
-0.275
361164
a0001 a0004 a0008
a0001c0001 a0001c0006 a0001c0013 a0004c0007 a0004c0009 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0004c0007t0001 others(6): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0046 others(59): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Hide
0.082
102
107
10
chr14_50900610_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50900610:splice
50900610:variant
goto
ABHD12Bintron_variantc.781-1219C>T
PYGL
Skin_Sun_Exposed_Lower_leg
5.725
-0.268
361164
a0001 a0004 a0008
a0001c0001 a0001c0006 a0001c0013 a0004c0007 a0004c0009 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0004c0007t0001 others(6): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0046 others(59): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Hide
0.081
114
121
10
chr14_50900610_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50900610:splice
50900610:variant
goto
ABHD12Bintron_variantc.781-1219C>T
PYGL
Stomach
6.920
-0.252
361164
a0001 a0004 a0008
a0001c0001 a0001c0006 a0001c0013 a0004c0007 a0004c0009 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0004c0007t0001 others(6): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0046 others(59): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Hide
0.093
70
76
10
chr14_50900610_C_T_b38
+
MODIFIER
chr14
C
T
TogoVar
50900610:splice
50900610:variant
goto
ABHD12Bintron_variantc.781-1219C>T
PYGL
Whole_Blood
7.369
0.108
361164
a0001 a0004 a0008
a0001c0001 a0001c0006 a0001c0013 a0004c0007 a0004c0009 others(1): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0006t0001 a0001c0013t0003 a0004c0007t0001 others(6): Hide
a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0046 others(59): Hide
HG00280.hp2 HG00408.hp1 HG00423.hp1 HG00544.hp2 HG00558.hp2 others(62): Hide
0.082
123
132
10
chr14_50900610_C_T_b38
+
MODIFIER
chr14
C
T
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
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
PYGL
Esophagus_Mucosa
32.848
-0.413
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
PYGL
Heart_Left_Ventricle
8.047
0.190
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
0.313
242
282
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Lung
6.029
0.127
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
0.306
314
368
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Skin_Sun_Exposed_Lower_leg
4.160
0.131
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
408
479
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
ABHD12B
Spleen
5.854
-0.269
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
0.343
159
190
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Spleen
6.118
0.128
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
0.343
159
190
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
ABHD12B
Whole_Blood
5.232
-0.111
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
0.313
430
501
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50902202:splice
50902202:variant
goto
ABHD12Bintron_variantc.863+293delT
PYGL
Whole_Blood
9.217
0.074
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
0.313
430
501
10
chr14_50902202_CT_C_b38
+
MODIFIER
chr14
CT
C
TogoVar
50905380:splice
50905380:variant
goto
ABHD12Bdownstream_gene_variantc.*1015del others(6): Hide
PYGL
Adipose_Subcutaneous
12.113
0.157
71330203
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(198): Hide
HG00280.hp2 HG00408.hp1 HG00408.hp2 HG00423.hp1 HG00423.hp2 others(211): Hide
0.326
396
463
10
chr14_50905380_CA_C_b38
+
MODIFIER
chr14
CA
C
TogoVar
50905380:splice
50905380:variant
goto
ABHD12Bdownstream_gene_variantc.*1015del others(6): Hide
PYGL
Adipose_Visceral_Omentum
6.508
0.134
71330203
a0001 a0002 a0004 a0005 a0008 others(2): Hide
a0001c0001 a0001c0005 a0001c0006 a0001c0011 a0001c0013 others(8): Hide
a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 a0001c0005t0004 a0001c0005t0007 others(25): Hide