chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
15938207
15938208
T
C
7
GENIC
homozygous
45097830
X
15939137
15939138
T
C
13
GENIC
homozygous
45097831
X
15940181
15940182
A
-
8
GENIC
homozygous
45097832
X
15940285
15940287
AC
--
12
GENIC
homozygous
45097833
X
15940480
15940481
G
T
19
GENIC
homozygous
45097834
X
15941046
15941047
T
C
21
GENIC
homozygous
45097835
X
15941323
15941324
T
TTAAAAAGTAGATGGGGGCTGGAGAGATGGCTCAGCCGTTAAAGGCTAGGCTCACAACCAAAAATA
7
GENIC
homozygous
45501287
X
15942121
15942122
G
A
7
GENIC
homozygous
45097836
X
15942703
15942704
C
-
4
GENIC
homozygous
45097837
X
15942713
15942714
G
-
4
GENIC
homozygous
45097838
X
15942725
15942726
C
G
4
GENIC
homozygous
45252136
X
15942764
15942765
G
T
4
GENIC
homozygous
45097839
X
15942850
15942851
T
C
1
GENIC
homozygous
45097842
X
15944405
15944406
T
TG
2
GENIC
heterozygous
45501289
X
15944408
15944409
G
GGGGCTCGAGACCCCAAAAGTACAAC
2
GENIC
heterozygous
45501291
X
15944791
15944792
T
C
8
GENIC
homozygous
45097844
X
15944801
15944802
G
A
8
GENIC
homozygous
45097845
X
15944858
15944859
A
-
8
GENIC
heterozygous
45501295
X
15944950
15944951
C
T
11
GENIC
homozygous
45097847
X
15945284
15945285
G
-
9
GENIC
homozygous
45097848
X
15946520
15946521
C
T
17
GENIC
homozygous
45097849
