chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
44703991
44703992
C
-
25
GENIC
homozygous
52611974
8
44705782
44705783
C
CAG
18
GENIC
homozygous
52611990
8
44706135
44706136
C
CT
17
GENIC
heterozygous
53505920
8
44706136
44706137
T
-
17
GENIC
heterozygous
53181455
8
44727740
44727741
G
GCTCCACTCCCCAGAAAGCACTGATCTACCTTACTCCTCC
40
GENIC
homozygous
53363368
8
44729987
44729988
C
CA
16
GENIC
possibly homozygous
53575698
8
44750695
44750696
C
T
19
GENIC
heterozygous
52612189
8
44750839
44750841
TG
--
5
GENIC
heterozygous
53429102
8
44758985
44758986
C
-
1
GENIC
homozygous
53460082
8
44774630
44774631
A
-
13
GENIC
heterozygous
52612379
8
44790964
44790965
G
-
30
GENIC
homozygous
52612574
8
44818861
44818862
C
T
13
GENIC
homozygous
52612738
8
44818863
44818864
A
T
11
GENIC
homozygous
52612740
8
44818867
44818868
G
T
11
GENIC
homozygous
52612742
8
44838380
44838381
A
-
24
GENIC
heterozygous
52968628
8
44850987
44850988
A
AT
11
GENIC
heterozygous
52613010
8
44856088
44856090
AC
--
14
GENIC
heterozygous
52613041
8
44868221
44868222
A
AG
11
GENIC
homozygous
52613082
8
44868222
44868223
C
CCCT
11
GENIC
homozygous
53379879
8
44868228
44868234
GGGGGT
------
9
GENIC
homozygous
53379881
8
44868239
44868240
T
G
6
GENIC
homozygous
53379883
8
44868240
44868241
G
T
6
GENIC
homozygous
53379885
8
44868242
44868243
G
C
6
GENIC
homozygous
53379887
8
44868250
44868251
C
A
4
GENIC
homozygous
52613086
8
44868262
44868263
G
A
1
GENIC
homozygous
53105636
