chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
109707884
109707885
T
C
28
GENIC
homozygous
116983819
10
109707985
109707996
CGCTCGAGGAC
42
GENIC
homozygous
132148046
10
109708375
109708376
G
A
26
GENIC
homozygous
116909707
10
109708616
109708617
A
G
41
GENIC
homozygous
116909709
10
109710993
109710994
C
A
37
GENIC
homozygous
116909710
10
109712254
109712254
T
57
GENIC
homozygous
132148047
10
109712255
109712256
A
C
60
GENIC
homozygous
116909711
10
109712825
109712825
CACACACACACA
28
GENIC
possibly homozygous
132148048
10
109714738
109714738
CTGGGCTGTGGGTCAGGTTGCCCATTCTTGGCTGAATGC
33
GENIC
homozygous
132148049
10
109714779
109714780
C
T
38
GENIC
homozygous
116909712
10
109715206
109715207
C
T
39
GENIC
homozygous
116909713
10
109716180
109716181
A
T
33
GENIC
possibly homozygous
116961940
10
109711454
109711455
A
G
35
GENIC
homozygous
116719021
10
109714734
109714735
T
C
45
GENIC
homozygous
117072051