chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
123550632
123550633
C
T
19
GENIC
homozygous
45362206
X
123551546
123551547
C
G
19
GENIC
homozygous
45214434
X
123551834
123551835
C
T
7
GENIC
homozygous
45214435