chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
101214365
101214366
G
33
GENIC
homozygous
127408706
1
101215139
101215139
T
63
GENIC
homozygous
132530266
1
101216069
101216070
A
G
64
GENIC
homozygous
108900040
1
101216070
101216071
A
G
64
GENIC
homozygous
108900042
1
101216531
101216532
A
C
45
GENIC
homozygous
108900044
1
101216814
101216815
G
A
29
GENIC
homozygous
108900045
1
101216892
101216893
G
C
11
GENIC
homozygous
108900047
1
101217815
101217816
C
T
54
GENIC
possibly homozygous
108900051
1
101219454
101219455
T
G
43
GENIC
homozygous
108900053
1
101219472
101219473
T
C
41
GENIC
homozygous
108900054
1
101219907
101219907
C
49
GENIC
homozygous
132530267
1
101219936
101219936
A
40
GENIC
homozygous
132530268
1
101219979
101219980
C
T
36
GENIC
homozygous
108900056
1
101220337
101220338
G
T
49
GENIC
homozygous
108900058
1
101221462
101221463
G
A
62
GENIC
possibly homozygous
108900060
1
101221956
101221957
G
A
65
GENIC
homozygous
108900062
1
101222515
101222516
A
G
69
GENIC
homozygous
108900064
1
101223973
101223973
TC
28
GENIC
heterozygous
132530269
1
101223974
101223974
C
31
GENIC
heterozygous
132530270
1
101225183
101225184
A
G
45
GENIC
possibly homozygous
108900065
1
101225567
101225567
TGTCTGTC
55
GENIC
homozygous
132530271
1
101225708
101225708
T
55
GENIC
possibly homozygous
132530272
1
101225841
101225842
T
C
73
GENIC
homozygous
108900067
1
101225893
101225894
C
T
62
GENIC
homozygous
108900069
1
101227251
101227252
A
G
42
GENIC
homozygous
108900070
1
101227349
101227350
C
T
48
GENIC
homozygous
108900072
1
101227478
101227479
C
T
52
GENIC
homozygous
108900074
1
101228567
101228568
T
C
45
GENIC
homozygous
108900076
1
101228981
101228982
C
T
55
GENIC
homozygous
108900078
1
101217497
101217497
GCCACCCAGAGAGAAAGACACATTCATGAGGTAGGGCCAGAATGAGACCCAGAGTCAGTGAAACC
1
GENIC
homozygous
133799524
