chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
108813877
108813877
A
9
GENIC
homozygous
127916582
3
108813879
108813879
A
9
GENIC
homozygous
127916583
3
108813899
108813900
T
11
GENIC
homozygous
127916584
3
108813940
108813941
A
15
GENIC
homozygous
127916585
3
108813942
108813943
T
15
GENIC
homozygous
127916586
3
108813974
108813977
TAT
16
GENIC
homozygous
127916587
3
108813979
108813982
AAG
16
GENIC
homozygous
127916588
3
108814000
108814001
G
15
GENIC
homozygous
127916589
3
108814016
108814017
A
15
GENIC
homozygous
127916590
3
108814060
108814061
C
7
GENIC
homozygous
127916591
3
108814070
108814070
G
6
GENIC
homozygous
127916592
3
108814073
108814074
T
6
GENIC
homozygous
127916593
3
108814086
108814087
C
6
GENIC
homozygous
127916594
3
108829634
108829635
G
19
GENIC
homozygous
127916598
3
108856611
108856645
GGTCACTCTACCAAATTGACATGAATTAACCACC
17
GENIC
homozygous
127916606
