chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
54555662
54555663
C
T
46
GENIC
homozygous
136707330
3
54556234
54556235
A
G
51
GENIC
homozygous
136707331
3
54556473
54556474
A
30
GENIC
possibly homozygous
136563122
3
54556476
54556481
TGTAT
30
GENIC
homozygous
136563123
3
54556501
54556508
GCGCGCG
36
GENIC
homozygous
136563124
3
54556509
54556510
G
A
37
GENIC
homozygous
136707332
3
54557709
54557710
C
A
36
GENIC
homozygous
136707333
3
54558737
54558737
AGGA
57
GENIC
homozygous
136563125
3
54558831
54558838
AAAATAA
44
GENIC
homozygous
136563126
3
54560001
54560002
C
G
45
GENIC
homozygous
136707334
3
54560150
54560151
A
G
53
GENIC
homozygous
136707335
3
54561135
54561136
T
C
63
GENIC
homozygous
136707336
3
54561509
54561510
C
T
68
GENIC
homozygous
136707337
3
54557521
54557521
CTGC
20
GENIC
heterozygous
148681751
3
54557522
54557522
AAGCTTCTGTAAGGCAAAGGACACTGTGGTTAGGACAAAACGGCAACCAAC
21
GENIC
heterozygous
148681752
