chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
153632002
153632003
G
-
17
GENIC
homozygous
45248875
X
153632108
153632110
CA
--
3
GENIC
homozygous
45532311
X
153633802
153633803
T
-
10
GENIC
homozygous
45322105
X
153634613
153634614
C
CTGAAGCTGTGGGGTAAGGGTGGACAAAGTTTTGCTGGACACAGTGGCTTATGCCTGTAATTCTAGCATTT
13
GENIC
homozygous
45486709
X
153642544
153642545
A
-
6
GENIC
heterozygous
45248886
X
153647276
153647278
AC
--
2
GENIC
heterozygous
45270322
X
153647900
153647901
C
CA
23
GENIC
homozygous
45248889
X
153647907
153647908
C
CA
21
GENIC
homozygous
45248890
X
153655014
153655015
C
A
20
GENIC
homozygous
45248894
X
153655051
153655052
G
-
17
GENIC
homozygous
45248895
X
153655058
153655059
C
-
18
GENIC
homozygous
45248896
X
153655068
153655069
C
-
19
GENIC
homozygous
45248897
X
153655098
153655099
C
-
13
GENIC
homozygous
45248898
X
153655120
153655121
T
-
13
GENIC
homozygous
45248899
X
153655125
153655126
G
A
12
GENIC
homozygous
45248900
X
153665825
153665827
GT
--
5
GENIC
heterozygous
45532315
X
153668312
153668314
TG
--
4
GENIC
heterozygous
45248916
