chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
116440435
116440436
A
G
20
GENIC
homozygous
116669365
8
116442167
116442168
G
A
20
GENIC
homozygous
116988081
8
116445025
116445026
C
T
21
GENIC
homozygous
116988082
8
116445837
116445838
A
T
20
GENIC
homozygous
116988083
8
116443385
116443386
C
A
6
GENIC
homozygous
116886467
8
116447898
116447899
T
C
18
GENIC
homozygous
116669375
8
116452145
116452146
G
A
21
GENIC
homozygous
116988084
8
116452714
116452715
A
24
GENIC
homozygous
128634996
8
116455245
116455246
G
A
30
GENIC
homozygous
116669383
8
116456152
116456153
A
T
21
GENIC
homozygous
116886475
8
116456155
116456156
T
A
21
GENIC
homozygous
116988085
8
116457515
116457516
C
T
19
GENIC
homozygous
116886479
8
116457555
116457556
G
C
16
GENIC
homozygous
116988086
8
116458088
116458089
G
A
3
GENIC
homozygous
116988087
8
116458524
116458525
A
G
22
GENIC
homozygous
116886489
8
116460232
116460233
A
G
15
GENIC
homozygous
116988089
8
116460459
116460460
G
T
28
GENIC
homozygous
116988090
8
116460661
116460662
T
C
20
GENIC
homozygous
116886493
8
116460716
116460717
C
T
22
GENIC
homozygous
116886495
8
116460860
116460861
C
G
22
GENIC
homozygous
116886497
8
116461203
116461204
T
G
25
GENIC
homozygous
116886499
8
116461338
116461339
T
A
19
GENIC
homozygous
117920113
8
116461784
116461785
A
G
23
GENIC
homozygous
116669391
8
116462564
116462565
G
C
30
GENIC
homozygous
116988091
8
116463353
116463354
C
T
25
GENIC
homozygous
116886501
8
116464151
116464152
T
C
25
GENIC
homozygous
116669399
8
116465370
116465371
T
C
18
GENIC
homozygous
116669401
8
116457904
116457937
TCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCC
7
GENIC
homozygous
132669862
8
116460990
116460993
CTT
19
GENIC
homozygous
132669863
8
116461336
116461337
C
18
GENIC
homozygous
132669864
8
116466228
116466228
G
13
GENIC
homozygous
132669865
8
116463170
116463171
T
G
15
GENIC
homozygous
116988092
