chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
106845394
106845395
A
T
18
GENIC
homozygous
138409184
8
106846351
106846352
T
C
12
GENIC
homozygous
138409185
8
106848311
106848312
G
A
19
GENIC
homozygous
142098966
8
106848712
106848713
G
A
26
GENIC
homozygous
138409190
8
106849882
106849883
A
G
22
GENIC
homozygous
142098967
8
106850072
106850073
G
A
16
GENIC
homozygous
142098968
8
106850107
106850108
G
A
16
GENIC
homozygous
142098969
8
106850117
106850118
T
C
19
GENIC
homozygous
142098970
8
106850152
106850153
A
G
21
GENIC
homozygous
142098971
8
106850372
106850373
A
G
23
GENIC
homozygous
138409192
8
106850397
106850398
A
T
27
GENIC
homozygous
142098972
8
106850530
106850531
T
G
33
GENIC
homozygous
142098973
8
106850591
106850592
G
A
26
GENIC
homozygous
142098974
8
106850659
106850660
T
G
23
GENIC
homozygous
138409193
8
106850666
106850667
G
T
23
GENIC
homozygous
142098975
8
106850789
106850790
T
C
28
GENIC
homozygous
142098976
8
106851500
106851501
C
G
28
GENIC
homozygous
142098977
8
106851747
106851748
G
A
18
GENIC
homozygous
142098978
8
106852098
106852099
A
T
21
GENIC
homozygous
142098979
8
106852243
106852244
T
C
10
GENIC
homozygous
142098980
8
106853057
106853058
G
A
17
GENIC
homozygous
142098981
8
106853600
106853601
T
A
27
GENIC
possibly homozygous
138409194
8
106854335
106854336
C
T
18
GENIC
homozygous
138409195
8
106856515
106856516
G
A
22
GENIC
homozygous
142098982
8
106856848
106856849
A
T
22
GENIC
homozygous
138409196
8
106857747
106857748
G
C
31
GENIC
homozygous
142098983
8
106849653
106849653
TG
16
GENIC
homozygous
142030123
8
106850189
106850191
TG
18
GENIC
homozygous
142030124
8
106852284
106852284
GAA
13
GENIC
homozygous
142030125
8
106853239
106853239
AATGATGATGATGATGATGACGATGAC
27
GENIC
homozygous
142030126
