chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
33996396
33996397
C
G
7
GENIC
homozygous
45284103
X
33996435
33996436
T
TATTTGTATAAATACACATGCATGTGTCAAA
1
GENIC
homozygous
45795693
X
33996493
33996494
A
G
11
GENIC
possibly homozygous
45284104
X
33996530
33996531
C
T
17
GENIC
possibly homozygous
45284105
X
33996745
33996746
G
GA
4
GENIC
homozygous
45284106
X
33996805
33996806
A
ACAGT
1
GENIC
homozygous
45284107
X
33997529
33997530
T
C
10
GENIC
possibly homozygous
45284108
X
33997628
33997629
C
T
8
GENIC
homozygous
45284109
X
33999175
33999176
A
G
18
GENIC
heterozygous
45284110
X
33999418
33999419
T
C
9
GENIC
homozygous
45284111
X
33999770
33999771
A
AC
4
GENIC
homozygous
45284113
X
34000213
34000214
G
A
6
GENIC
homozygous
45284114
X
34001172
34001173
C
T
11
GENIC
homozygous
45284115
X
34001642
34001643
T
G
10
GENIC
homozygous
45284116
X
34002377
34002378
G
A
17
GENIC
possibly homozygous
45284117
X
34002803
34002804
C
T
13
GENIC
possibly homozygous
45284118
X
34005642
34005643
C
G
14
GENIC
possibly homozygous
45284120
X
34005774
34005775
G
A
12
GENIC
possibly homozygous
45284121
X
34007465
34007466
T
C
3
GENIC
homozygous
45284124
X
34007710
34007711
T
TA
2
GENIC
heterozygous
45284125
X
34007976
34007977
T
TAAA
1
GENIC
homozygous
45284126
X
34008141
34008143
TA
--
11
GENIC
homozygous
45284127
X
34008423
34008424
A
T
7
GENIC
heterozygous
45284128
X
34009166
34009167
G
T
3
GENIC
homozygous
45122432
X
34006356
34006357
T
-
2
GENIC
homozygous
45122429
X
34009118
34009119
G
A
2
GENIC
homozygous
45122430
X
34009353
34009354
C
G
9
GENIC
homozygous
45284130
X
34009708
34009712
CCTG
----
2
GENIC
homozygous
45284131
X
34010135
34010136
G
C
10
GENIC
possibly homozygous
45284132
X
34010504
34010505
A
-
8
GENIC
heterozygous
45630876
X
34010542
34010543
A
C
5
GENIC
homozygous
45284133
X
34011348
34011349
G
T
11
GENIC
homozygous
45284134
X
34012170
34012171
A
AG
2
GENIC
heterozygous
45122434
