chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
205778169
205778173
TTTG
22
GENIC
homozygous
127476431
1
205780823
205780824
A
G
16
GENIC
homozygous
108515513
1
205782782
205782783
A
G
21
GENIC
homozygous
108515514
1
205783066
205783067
T
A
20
GENIC
homozygous
108515515
1
205783216
205783217
T
C
16
GENIC
homozygous
108515516
1
205783831
205783832
A
G
13
GENIC
homozygous
108515517
1
205783841
205783842
G
A
13
GENIC
homozygous
108515518
1
205784212
205784213
A
G
14
GENIC
homozygous
108515519
1
205784348
205784349
T
C
16
GENIC
homozygous
108515520
1
205784700
205784701
A
11
GENIC
homozygous
127476432
1
205784723
205784724
C
A
17
GENIC
homozygous
108515521
1
205785019
205785020
C
G
19
GENIC
possibly homozygous
108515522
1
205785504
205785505
C
T
15
GENIC
homozygous
108515523
1
205785568
205785569
T
C
15
GENIC
homozygous
108515524
1
205785948
205785948
C
19
GENIC
homozygous
127476433
1
205786087
205786088
A
G
21
GENIC
homozygous
108515525
1
205787279
205787309
GCTGTGTCCCTTGTGTAGACAGGCATGCTG
20
GENIC
homozygous
127476434
1
205787562
205787563
C
T
22
GENIC
homozygous
108515527
1
205787607
205787608
A
T
25
GENIC
homozygous
108515528
1
205787622
205787623
G
A
25
GENIC
homozygous
108515529
1
205788631
205788632
T
C
21
GENIC
homozygous
108515530
1
205789330
205789331
T
G
22
GENIC
homozygous
108515531
1
205789682
205789683
G
A
13
GENIC
homozygous
108515532
