chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
115622180
115622181
A
G
46
GENIC
homozygous
45199852
X
115622388
115622389
C
CTTGG
5
GENIC
homozygous
45521950
X
115622391
115622392
A
ATTTAGCTCAGTGGTAGAGCGCTTGCCTAGC
4
GENIC
homozygous
45521953
X
115624428
115624437
AAAAAAAAA
---------
12
GENIC
homozygous
45199858
X
115624626
115624627
T
G
60
GENIC
homozygous
45199859
X
115624642
115624643
C
T
61
GENIC
homozygous
45199860
X
115625627
115625628
T
-
32
GENIC
possibly homozygous
45199861
X
115625722
115625723
C
A
44
GENIC
homozygous
45199862
X
115626127
115626128
T
TAA
22
GENIC
possibly homozygous
45199863
X
115626127
115626128
T
TA
22
GENIC
heterozygous
45199864
X
115626583
115626584
C
A
45
GENIC
homozygous
45199865
X
115626623
115626624
T
C
54
GENIC
homozygous
45199866
X
115627032
115627033
C
CA
21
GENIC
possibly homozygous
45521955
