chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
50414784
50414785
C
CAAAAAA
15
GENIC
heterozygous
50546908
12
50419050
50419051
T
TGCTA
1
GENIC
homozygous
50546909
12
50419078
50419079
A
AAG
8
GENIC
homozygous
50513900
12
50419079
50419080
C
CGCTCTACCACTGAGCTAAATCCCCAA
9
GENIC
homozygous
50513902
12
50430513
50430514
A
AAAAC
31
GENIC
homozygous
50238275
12
50436001
50436002
C
CAG
29
GENIC
homozygous
50238310