chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
1215434
1215435
G
A
34
GENIC
homozygous
140602100
X
1216346
1216346
TC
26
GENIC
possibly homozygous
140574019
X
1217598
1217599
A
C
35
GENIC
homozygous
140602101