chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
247502531
247502532
C
T
17
GENIC
homozygous
109017655
1
247503300
247503301
A
C
20
GENIC
homozygous
108775547
1
247503323
247503324
C
T
19
GENIC
homozygous
108775548
1
247503327
247503328
C
T
19
GENIC
homozygous
108775549
1
247505170
247505171
A
C
17
GENIC
homozygous
108602890
1
247505282
247505283
C
T
12
GENIC
homozygous
108602891
1
247505976
247505977
T
A
25
GENIC
homozygous
108602892
1
247507426
247507427
T
A
15
GENIC
homozygous
108602897
1
247508430
247508431
G
T
12
GENIC
homozygous
108602898
1
247508947
247508965
CAGTGGATTCCCGACACT
15
GENIC
homozygous
127501463
1
247509726
247509727
A
C
29
GENIC
homozygous
109017657
1
247510104
247510105
C
G
21
GENIC
homozygous
108602899
1
247510190
247510191
C
T
22
GENIC
homozygous
109017658
1
247511468
247511469
A
G
25
GENIC
homozygous
108602902
1
247511571
247511572
A
G
32
GENIC
homozygous
108602903
1
247512289
247512290
T
C
26
GENIC
homozygous
108602904
1
247512314
247512314
T
26
GENIC
homozygous
127501467
1
247513265
247513265
TTCCCTCCGTCCCTTGACCTGTTCTA
23
GENIC
homozygous
131265587
1
247513612
247513613
C
A
21
GENIC
homozygous
109017659
1
247514372
247514373
G
A
30
GENIC
homozygous
109017660
1
247514378
247514379
G
A
32
GENIC
homozygous
108602907
