chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
115622388
115622389
C
CTTGG
3
GENIC
homozygous
45521950
X
115622391
115622392
A
ATTTAGCTCAGTGGTAGAGCGCTTGCCTAGC
5
GENIC
homozygous
45521953
X
115622401
115622402
G
GCA
9
GENIC
homozygous
45550953
