chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
50286895
50286896
C
G
49
GENIC
possibly homozygous
115351952
12
50287755
50287756
T
A
32
GENIC
homozygous
115351954
12
50288367
50288368
T
G
36
GENIC
homozygous
115351956
12
50288443
50288444
C
A
53
GENIC
homozygous
115351958
12
50289086
50289087
T
G
29
GENIC
homozygous
115351960
12
50291593
50291594
T
A
54
GENIC
homozygous
115351962
12
50294439
50294440
T
C
25
GENIC
heterozygous
131722699
12
50300607
50300608
A
T
49
GENIC
homozygous
115351964
12
50306573
50306574
G
A
40
GENIC
homozygous
115351966
12
50292303
50292315
GCCAGGAGCTGG
50
GENIC
homozygous
129001228
12
50294249
50294250
G
58
GENIC
homozygous
129001229
12
50295961
50296041
GCAGCAGCAGCAGGAGCAGCCAGAGCCTACAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCCAGAGCCTACAGCAGCA
26
GENIC
homozygous
129001230
12
50298303
50298303
TC
58
GENIC
homozygous
129001231
12
50292669
50292670
G
A
56
GENIC
homozygous
115444425
12
50310633
50310634
T
C
9
GENIC
homozygous
115351968
12
50311404
50311405
T
C
37
GENIC
homozygous
115351970
12
50311497
50311498
T
C
45
GENIC
possibly homozygous
115351972
12
50314381
50314381
CA
36
GENIC
homozygous
129001233
