chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
100513165
100513166
T
C
59
GENIC
homozygous
141519400
3
100513289
100513290
C
T
69
GENIC
homozygous
141519401
3
100513333
100513334
G
A
76
GENIC
homozygous
141519402
3
100513474
100513475
G
A
57
GENIC
homozygous
141519403
3
100514096
100514097
G
A
59
GENIC
homozygous
141519404
3
100514277
100514278
C
G
55
GENIC
homozygous
141519405
3
100514385
100514386
A
G
42
GENIC
homozygous
141519406
3
100514490
100514491
T
A
55
GENIC
homozygous
141519407
3
100514849
100514850
A
G
61
GENIC
homozygous
141519408
3
100515146
100515147
A
T
58
GENIC
homozygous
141519409
3
100518857
100518858
G
A
46
GENIC
possibly homozygous
154127425
3
100519976
100519977
C
T
50
GENIC
homozygous
141519410
3
100522048
100522049
C
G
22
GENIC
homozygous
141519413
3
100523618
100523619
T
A
62
GENIC
homozygous
141519414
3
100518857
100518858
G
46
GENIC
heterozygous
145395305
3
100520852
100520853
C
30
GENIC
homozygous
403071710
3
100520852
100520853
C
T
30
GENIC
heterozygous
403071711
3
100522056
100522057
C
19
GENIC
heterozygous
403071713
3
100522056
100522057
C
G
19
GENIC
homozygous
403071714
3
100520833
100520865
TTATTTATTTATTTATTTACTTACTTACTTAC
30
GENIC
homozygous
141477379