chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
129708044
129708045
A
AT
3
GENIC
homozygous
57670662
3
129708285
129708286
A
AG
18
GENIC
possibly homozygous
57670664
3
129708608
129708609
G
T
22
GENIC
possibly homozygous
57670666
3
129708637
129708638
A
G
34
GENIC
possibly homozygous
57670668
3
129708791
129708792
A
T
6
GENIC
homozygous
57670670
3
129708793
129708794
A
AGCTGTC
3
GENIC
homozygous
57670672
3
129708795
129708796
G
C
3
GENIC
homozygous
57670674
3
129709807
129709808
T
C
23
GENIC
homozygous
57670678
3
129710892
129710893
C
T
15
GENIC
possibly homozygous
57670682
3
129711221
129711222
G
A
9
GENIC
heterozygous
57670684
3
129711437
129711438
C
T
6
GENIC
homozygous
57670686
3
129711716
129711717
T
A
22
GENIC
possibly homozygous
57670688
3
129712146
129712147
T
G
21
GENIC
possibly homozygous
57670692
3
129712681
129712682
C
CATGCCT
2
GENIC
homozygous
57670694
3
129712774
129712775
C
T
24
GENIC
homozygous
57670696
3
129713653
129713654
A
T
25
GENIC
homozygous
57670699
3
129714047
129714048
A
G
9
GENIC
homozygous
57670701
3
129715054
129715055
G
A
14
GENIC
homozygous
57670709
3
129715229
129715230
C
CA
3
GENIC
heterozygous
57670711
3
129715270
129715271
A
G
10
GENIC
possibly homozygous
57670713
3
129715333
129715334
T
TAG
17
GENIC
homozygous
57670715
3
129715518
129715519
C
T
19
GENIC
homozygous
57670717
3
129715599
129715600
G
A
19
GENIC
possibly homozygous
57670719
3
129716465
129716466
C
CCTGCCT
5
GENIC
homozygous
57670721
3
129716495
129716497
TT
--
1
GENIC
homozygous
58695715
3
129718300
129718345
CTGCATATATGTCATGGTTGTGCAGCTAGAGTCTGAGCTGGGTCT
---------------------------------------------
32
GENIC
heterozygous
58751728
