chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
15
44791276
44791277
C
T
16
GENIC
homozygous
139726731
15
44792258
44792259
A
G
28
GENIC
homozygous
139726732
15
44794307
44794308
C
T
36
GENIC
homozygous
139726733
15
44794541
44794542
G
A
23
GENIC
homozygous
139726734
15
44795141
44795142
G
C
15
GENIC
homozygous
139726735
15
44795160
44795161
G
C
18
GENIC
homozygous
139726736
15
44795960
44795961
C
T
34
GENIC
homozygous
139726737
15
44796357
44796358
A
32
GENIC
homozygous
139632084
15
44798780
44798782
AT
27
GENIC
possibly homozygous
139632085
15
44799151
44799151
CAAAGATGCATATGCACAGATCTAG
20
GENIC
homozygous
139632086
15
44799267
44799268
G
C
30
GENIC
homozygous
139726738
15
44799413
44799414
T
C
24
GENIC
homozygous
139726739
15
44799477
44799478
G
A
27
GENIC
homozygous
139726740
15
44800094
44800095
G
A
26
GENIC
homozygous
139726741
15
44800100
44800101
A
G
27
GENIC
homozygous
139726742
15
44800363
44800369
TGTCTG
20
GENIC
homozygous
139632087
15
44800380
44800381
C
G
16
GENIC
homozygous
139726743
15
44800382
44800383
C
G
16
GENIC
homozygous
139726744
15
44800384
44800385
C
G
14
GENIC
homozygous
139726745
15
44800386
44800387
C
G
13
GENIC
homozygous
139726746
15
44800388
44800389
C
G
13
GENIC
homozygous
139726747
15
44800390
44800391
C
G
12
GENIC
homozygous
139726748
15
44800392
44800393
C
G
11
GENIC
homozygous
139726749
15
44801825
44801826
G
A
36
GENIC
homozygous
139726750
15
44803191
44803192
G
A
27
GENIC
homozygous
139726751
15
44803273
44803274
C
A
26
GENIC
homozygous
139726752
15
44804140
44804141
C
T
27
GENIC
homozygous
139726753
15
44805312
44805315
TTC
30
GENIC
homozygous
139632088
15
44805316
44805317
G
31
GENIC
homozygous
139632089
15
44805318
44805319
G
A
32
GENIC
homozygous
139726754
15
44798781
44798782
T
27
GENIC
possibly homozygous
403855536
15
44798781
44798782
T
C
27
GENIC
heterozygous
154890494
