chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
107501578
107501579
T
G
31
GENIC
heterozygous
45192704
X
107502673
107502674
C
CT
12
GENIC
homozygous
45192705
X
107502684
107502685
G
T
10
GENIC
homozygous
45192706
X
107502687
107502688
C
A
9
GENIC
homozygous
45192707
