chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
59123147
59123148
C
T
35
GENIC
homozygous
116511053
8
59123153
59123154
C
A
35
GENIC
homozygous
116511055
8
59123188
59123189
T
C
42
GENIC
homozygous
116511057
8
59123193
59123194
T
C
44
GENIC
homozygous
116511059
8
59123521
59123522
A
G
45
GENIC
homozygous
116511061
8
59123570
59123571
T
56
GENIC
homozygous
128595528
8
59123871
59123872
T
C
30
GENIC
homozygous
116511063
8
59124563
59124564
T
C
58
GENIC
homozygous
116511065
8
59124615
59124616
G
A
61
GENIC
homozygous
116511067
8
59125238
59125239
A
G
62
GENIC
homozygous
116511069
8
59125935
59125936
T
A
39
GENIC
possibly homozygous
126704199
8
59129271
59129272
C
T
42
GENIC
homozygous
116511071
8
59130162
59130163
G
A
46
GENIC
homozygous
126704201
8
59131505
59131505
ACAG
40
GENIC
homozygous
130363024
8
59124910
59124911
T
C
17
GENIC
possibly homozygous
117157633
8
59124912
59124913
C
G
16
GENIC
possibly homozygous
117157634
8
59124920
59124921
G
T
15
GENIC
possibly homozygous
117157635
8
59124983
59124993
ACACACAGAC
45
GENIC
possibly homozygous
130363021
8
59129724
59129728
ACAT
45
GENIC
possibly homozygous
130363022
8
59130870
59130872
AA
52
GENIC
homozygous
130363023
8
59132175
59132176
G
A
31
GENIC
homozygous
116511087
8
59133387
59133388
A
G
67
GENIC
homozygous
116511089
8
59133665
59133666
T
C
62
GENIC
homozygous
116511091
8
59134060
59134061
C
T
61
GENIC
homozygous
116511093
8
59134417
59134418
G
A
56
GENIC
homozygous
116511095
8
59134550
59134551
G
A
62
GENIC
homozygous
126704202
8
59134665
59134666
G
A
52
GENIC
homozygous
126704203
8
59135521
59135565
GCTCCTCCTACATATTCCCAGAGCTCCTCCTACATATTCCCAGA
17
GENIC
homozygous
130363025
8
59136009
59136010
G
T
54
GENIC
homozygous
116511115
8
59136307
59136308
G
A
53
GENIC
homozygous
126704204
8
59136904
59136905
G
A
46
GENIC
homozygous
126704205
8
59138891
59138892
A
G
62
GENIC
homozygous
126704206
8
59139010
59139011
T
C
63
GENIC
homozygous
126704207
8
59139301
59139302
G
A
56
GENIC
homozygous
126704208
