chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
66071642
66071643
C
CTTTTCTT
2
GENIC
heterozygous
45478453
X
66071861
66071863
CA
--
15
GENIC
heterozygous
45478455
X
66073753
66073754
T
-
4
GENIC
heterozygous
45569530
X
66076245
66076252
GTCGCCG
-------
28
GENIC
homozygous
45145112
X
66076267
66076268
G
T
23
GENIC
homozygous
45145113
X
66076275
66076276
C
A
24
GENIC
homozygous
45145116
X
66076279
66076280
A
-
22
GENIC
homozygous
45145117
X
66076286
66076287
G
-
25
GENIC
homozygous
45145118
X
66076291
66076292
G
-
24
GENIC
homozygous
45145119
X
66076295
66076296
C
-
23
GENIC
homozygous
45145120
X
66076302
66076303
C
-
22
GENIC
homozygous
45145121
X
66076309
66076310
T
-
19
GENIC
homozygous
45145122
X
66076315
66076316
C
-
16
GENIC
homozygous
45145123
X
66076318
66076319
C
-
15
GENIC
homozygous
45145124
X
66076324
66076325
T
-
15
GENIC
homozygous
45145125
X
66076329
66076330
A
-
15
GENIC
homozygous
45145126
X
66076330
66076331
G
C
14
GENIC
homozygous
45510635
X
66076336
66076337
T
-
15
GENIC
homozygous
45145127
X
66076343
66076344
A
-
18
GENIC
homozygous
45145128
X
66076350
66076351
G
-
20
GENIC
homozygous
45145129
X
66083973
66083974
A
G
10
GENIC
homozygous
45145146
X
66083987
66083988
G
T
11
GENIC
homozygous
45145147
X
66084026
66084027
C
-
13
GENIC
homozygous
45145148
X
66084118
66084119
A
T
21
GENIC
homozygous
45145149
X
66084134
66084135
G
C
22
GENIC
homozygous
45145150
X
66084162
66084163
A
T
20
GENIC
homozygous
45145151
X
66084170
66084171
A
T
22
GENIC
homozygous
45145152
X
66084189
66084190
A
G
26
GENIC
homozygous
45145153
X
66084191
66084192
C
T
27
GENIC
homozygous
45145154
X
66099335
66099337
AC
--
14
GENIC
heterozygous
45569532
X
66121546
66121547
A
ACAGCTTCCGTAACAATCACCCTCTTCTTTTGTTTTGAGAAAACGTTTCATATTCTAGGCTGGTC
14
GENIC
possibly homozygous
45510639
X
66132143
66132145
AC
--
12
GENIC
heterozygous
45569534
