chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
59123147
59123148
C
T
42
GENIC
homozygous
116511053
8
59123153
59123154
C
A
40
GENIC
homozygous
116511055
8
59123188
59123189
T
C
39
GENIC
homozygous
116511057
8
59123193
59123194
T
C
43
GENIC
homozygous
116511059
8
59123521
59123522
A
G
64
GENIC
homozygous
116511061
8
59123570
59123571
T
64
GENIC
homozygous
128595528
8
59123871
59123872
T
C
45
GENIC
homozygous
116511063
8
59124563
59124564
T
C
53
GENIC
homozygous
116511065
8
59124615
59124616
G
A
55
GENIC
homozygous
116511067
8
59124910
59124911
T
C
28
GENIC
homozygous
117157633
8
59124912
59124913
C
G
28
GENIC
homozygous
117157634
8
59124920
59124921
G
T
28
GENIC
homozygous
117157635
8
59125238
59125239
A
G
63
GENIC
homozygous
116511069
8
59129271
59129272
C
T
43
GENIC
homozygous
116511071
8
59129690
59129691
A
G
26
GENIC
homozygous
116511083
8
59129692
59129693
A
G
26
GENIC
homozygous
116511085
8
59132175
59132176
G
A
23
GENIC
homozygous
116511087
8
59133387
59133388
A
G
56
GENIC
homozygous
116511089
8
59133665
59133666
T
C
66
GENIC
homozygous
116511091
8
59134060
59134061
C
T
57
GENIC
homozygous
116511093
8
59134417
59134418
G
A
66
GENIC
homozygous
116511095
8
59135580
59135581
A
T
16
GENIC
possibly homozygous
116511099
8
59135602
59135603
A
T
21
GENIC
heterozygous
116511103
8
59135624
59135625
T
A
7
GENIC
possibly homozygous
128661090
8
59135632
59135633
C
T
7
GENIC
possibly homozygous
128661091
8
59135713
59135867
CCCAGAGCTCCTCCTACATATTCCCAGAGTTCCTCCTACATATTCCCAGAGCTCCTCCTACATATTCCCAGAGCTCCTCCTACATATTCCCAGAGCTCCTCCTACATATACCCAGAGCTCCTCCTACATATACCCAGAGCTCCTCCTACATATA
13
GENIC
heterozygous
128595529
8
59136009
59136010
G
T
57
GENIC
homozygous
116511115
8
59136066
59136067
G
A
53
GENIC
homozygous
116511117
8
59136902
59136903
G
A
61
GENIC
homozygous
116511119
8
59137906
59137907
C
G
23
GENIC
heterozygous
128661092
8
59138199
59138200
C
G
71
GENIC
homozygous
116511121
8
59139625
59139626
C
A
70
GENIC
homozygous
116511123
