chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
148051662
148051663
A
C
30
GENIC
homozygous
119744147
3
148051667
148051668
G
A
30
GENIC
homozygous
119744148
3
148051693
148051693
G
29
GENIC
homozygous
131330105
3
148052796
148052797
T
C
48
GENIC
homozygous
112365090
3
148052654
148052655
T
C
49
GENIC
homozygous
112365088
3
148053383
148053385
AA
22
GENIC
homozygous
131330107
3
148053496
148053497
A
C
38
GENIC
possibly homozygous
112365092
3
148053848
148053849
T
C
58
GENIC
homozygous
112365093
3
148053865
148053867
CT
57
GENIC
homozygous
132822834
3
148054130
148054131
G
55
GENIC
homozygous
131330109
3
148054214
148054215
A
C
38
GENIC
homozygous
112365094
3
148054261
148054262
A
C
42
GENIC
homozygous
119744150
3
148054658
148054659
G
40
GENIC
homozygous
131330110
3
148054660
148054665
CACAG
41
GENIC
homozygous
131330111
3
148054744
148054744
G
36
GENIC
homozygous
133116846
3
148053942
148053943
C
48
GENIC
homozygous
133116843
3
148054520
148054521
G
63
GENIC
homozygous
133116844
3
148054560
148054574
GAGACAGAGACAGA
61
GENIC
homozygous
133116845
3
148054753
148054754
A
G
36
GENIC
homozygous
112365095
3
148054782
148054783
A
G
36
GENIC
homozygous
112365096
3
148055350
148055351
A
G
60
GENIC
possibly homozygous
112365097
3
148055406
148055407
C
T
55
GENIC
possibly homozygous
112365098
3
148055695
148055696
T
C
27
GENIC
homozygous
112365099
3
148055699
148055723
CTGCCTCTGCCTCTGCCTCTGCCT
25
GENIC
homozygous
133116847
3
148055927
148056043
CTCTGCCTCTGCCTCTGCCTCTCTGCCTCTCTGCCTCTGCCTCTGCCTCTGCCTCTGCCTCTGCCTCTGCCTCTGCCTCTGCCTCAGCCTCTCTGCCTCTGCCTCTGCCTCAGCCT
24
GENIC
homozygous
133116848
3
148056314
148056317
CAT
41
GENIC
homozygous
131330112
3
148057049
148057050
G
A
34
GENIC
homozygous
112365106
