chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
131090612
131090613
T
C
24
GENIC
homozygous
52896194
8
131091216
131091217
T
C
21
GENIC
homozygous
53065537
8
131093978
131093979
G
C
23
GENIC
homozygous
52896204
8
131094058
131094059
A
G
32
GENIC
possibly homozygous
52896207
8
131097872
131097873
C
CACATGTCACACAGATCTGTCTGAGCTCAGCTCACACATGTCACACAGATCCATCTGTGCTCAGCTCAT
92
GENIC
possibly homozygous
53415948
8
131101188
131101189
A
C
44
GENIC
homozygous
53065553
8
131101237
131101238
A
C
40
GENIC
homozygous
53065554
8
131102601
131102602
C
T
26
GENIC
homozygous
53727166
8
131103302
131103303
T
C
37
GENIC
homozygous
53065556
8
131103425
131103426
T
C
16
GENIC
homozygous
52896304
8
131103494
131103495
C
G
23
GENIC
homozygous
53065557
8
131104227
131104228
C
A
28
GENIC
homozygous
53065558
8
131104625
131104626
T
G
24
GENIC
homozygous
53065559
8
131104828
131104830
GT
--
2
GENIC
heterozygous
53415949
8
131105633
131105634
T
C
26
GENIC
homozygous
52896315
