chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
4
159675223
159675224
T
C
35
GENIC
homozygous
113185612
4
159675365
159675367
AG
37
GENIC
heterozygous
132607823
4
159676887
159676891
TGTA
11
GENIC
homozygous
132607824
4
159677223
159677224
A
T
4
GENIC
heterozygous
132618974
4
159677225
159677226
A
T
4
GENIC
heterozygous
132618975
4
159677273
159677273
AGAC
23
GENIC
homozygous
132607825
4
159679125
159679125
T
30
GENIC
possibly homozygous
130939973
4
159679238
159679239
A
G
41
GENIC
homozygous
113185613
4
159679923
159679924
G
A
42
GENIC
homozygous
113185614
4
159681922
159681922
CCCCTCCCCCCTCCCCCTTCCTTCCCCCTCCCTCCCCCCTCCCCCTTCCTTCC
4
GENIC
homozygous
128097694
4
159682204
159682205
C
T
37
GENIC
homozygous
113185615
4
159683154
159683155
C
G
36
GENIC
homozygous
113185616
4
159683183
159683184
C
T
37
GENIC
homozygous
113185617
4
159684403
159684404
C
T
41
GENIC
homozygous
113185619
4
159692800
159692801
G
T
22
GENIC
possibly homozygous
113185620
4
159693262
159693262
A
42
GENIC
possibly homozygous
130547168
4
159694753
159694754
C
T
48
GENIC
homozygous
113185621
4
159695086
159695087
G
T
37
GENIC
homozygous
113185622
