chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
247521717
247521718
T
C
38
GENIC
homozygous
108602910
1
247523590
247523590
A
47
GENIC
homozygous
127501468
1
247525392
247525392
GGGGTGTGTGTGTGTATGAGGGGTGTGTGTGTGTATGAGGGGTGTGTGC
15
GENIC
possibly homozygous
127501469
1
247525872
247525873
T
C
51
GENIC
homozygous
108602911
1
247526115
247526118
AAG
52
GENIC
homozygous
127501470
1
247530434
247530434
GTCCTCCCCAGCTGTGCTCACA
11
GENIC
possibly homozygous
127501471
1
247531941
247531942
T
C
49
GENIC
homozygous
108602912
1
247532262
247532263
T
C
46
GENIC
homozygous
108602913
1
247532539
247532540
G
C
59
GENIC
homozygous
108602914
1
247534313
247534314
T
A
48
GENIC
homozygous
108602915
1
247536407
247536408
G
A
50
GENIC
possibly homozygous
108602916
1
247536719
247536720
G
36
GENIC
possibly homozygous
127501472
1
247536779
247536781
AT
32
GENIC
heterozygous
127501473
1
247536789
247536790
A
G
34
GENIC
possibly homozygous
120476762
1
247537695
247537696
C
A
42
GENIC
homozygous
108602917
1
247537884
247537885
A
G
42
GENIC
homozygous
108602918
1
247539146
247539147
G
A
47
GENIC
homozygous
108602919
