chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
108415653
108415654
G
A
50
GENIC
homozygous
117136432
10
108415960
108415961
C
A
58
GENIC
homozygous
117136433
10
108416077
108416078
G
A
42
GENIC
homozygous
117136434
10
108416402
108416403
G
A
49
GENIC
homozygous
117136435
10
108416505
108416506
A
G
39
GENIC
homozygous
116908793
10
108415961
108415962
T
C
58
GENIC
homozygous
117145223
10
108418313
108418314
C
G
46
GENIC
homozygous
117145225
10
108416220
108416221
T
C
45
GENIC
homozygous
116715850
10
108417681
108417682
T
A
43
GENIC
homozygous
116715852
10
108418170
108418170
ACACAGGACGGGCC
51
GENIC
possibly homozygous
134229250
10
108418849
108418850
A
G
49
GENIC
homozygous
116715858
10
108418900
108418901
T
C
58
GENIC
homozygous
116715861
10
108419303
108419304
T
C
63
GENIC
possibly homozygous
116908800
10
108420294
108420295
G
C
41
GENIC
homozygous
116715863
10
108420753
108420754
A
G
59
GENIC
homozygous
116908805
10
108420813
108420814
G
A
64
GENIC
homozygous
117136436
10
108420888
108420898
GCCAAGTACC
51
GENIC
homozygous
134229251
10
108421113
108421114
G
A
58
GENIC
homozygous
117136437
10
108421143
108421144
T
C
66
GENIC
homozygous
116908808
10
108421148
108421149
G
A
65
GENIC
homozygous
117136438
10
108422041
108422042
A
G
49
GENIC
homozygous
116715867
10
108423089
108423090
A
T
62
GENIC
homozygous
117136439
10
108423293
108423294
A
G
59
GENIC
homozygous
116908809
10
108423371
108423372
A
G
61
GENIC
homozygous
116908810
10
108423745
108423746
A
C
68
GENIC
homozygous
116715869
10
108424434
108424435
C
A
42
GENIC
homozygous
117136440
10
108424489
108424489
CTTTAAAACATGACGAGGGGTTTCTTT
29
GENIC
homozygous
134229252
10
108424629
108424630
A
T
48
GENIC
homozygous
116908811
10
108424868
108424869
A
C
61
GENIC
homozygous
116908812
10
108420138
108420139
C
T
46
GENIC
homozygous
116961750
10
108420145
108420146
A
G
47
GENIC
homozygous
116961752
10
108420147
108420148
C
T
47
GENIC
homozygous
116961754
10
108424941
108424942
C
T
57
GENIC
homozygous
117136441
