chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
105568153
105568154
A
G
31
GENIC
homozygous
116837132
10
105568214
105568215
A
T
23
GENIC
homozygous
116837134
10
105568539
105568540
A
G
40
GENIC
homozygous
116837136
10
105568777
105568778
T
C
33
GENIC
homozygous
116837138
10
105569180
105569181
C
G
39
GENIC
homozygous
116837140
10
105569232
105569233
T
C
43
GENIC
homozygous
116837142
10
105569499
105569500
C
T
43
GENIC
homozygous
116837144
10
105569518
105569519
A
G
43
GENIC
homozygous
116837146
10
105569583
105569584
C
T
42
GENIC
homozygous
116837148
10
105569639
105569640
G
A
33
GENIC
homozygous
116837150
10
105569650
105569651
C
T
36
GENIC
homozygous
116837152
10
105569707
105569708
T
C
31
GENIC
homozygous
116837154
10
105570102
105570102
ATAT
10
GENIC
homozygous
133233631
10
105570119
105570120
G
5
GENIC
homozygous
133233632
10
105570121
105570154
TGCACACACACAGATACACACACACAGAGATGC
4
GENIC
homozygous
133233633
10
105570164
105570166
AC
5
GENIC
homozygous
133233634
10
105570176
105570178
AC
5
GENIC
homozygous
133233635
10
105570192
105570202
ACACACATAT
5
GENIC
homozygous
133233636
10
105570223
105570224
T
G
5
GENIC
homozygous
126489858
10
105570831
105570832
T
C
38
GENIC
homozygous
116837156
10
105571011
105571012
G
A
38
GENIC
homozygous
116837158
10
105571015
105571016
G
A
39
GENIC
homozygous
116837160
10
105572049
105572050
G
T
47
GENIC
possibly homozygous
116837162
10
105572123
105572124
C
G
55
GENIC
possibly homozygous
116837164
10
105572362
105572363
T
C
48
GENIC
homozygous
116837166