chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
32666616
32666617
G
A
32
GENIC
possibly homozygous
52566406
8
32667177
32667178
G
A
17
GENIC
homozygous
52566410
8
32667203
32667205
TT
--
8
GENIC
homozygous
52952789
8
32667222
32667223
T
C
13
GENIC
homozygous
52566413
8
32667363
32667364
C
G
24
GENIC
homozygous
52566416
8
32667456
32667457
T
C
18
GENIC
homozygous
52566422
8
32667527
32667528
T
-
21
GENIC
homozygous
52566425
8
32668262
32668263
T
TA
18
GENIC
homozygous
52566428
8
32668298
32668299
C
CTTTTTTTTTTT
12
GENIC
heterozygous
53375617
8
32668757
32668758
A
AG
29
GENIC
homozygous
52952791
8
32669348
32669349
G
C
29
GENIC
homozygous
52952793
8
32669797
32669813
CAACCAAACAAACAAA
----------------
10
GENIC
possibly homozygous
52566443
8
32670118
32670121
AAA
---
23
GENIC
possibly homozygous
52952795
8
32671157
32671158
T
-
12
GENIC
heterozygous
52952799
8
32671756
32671757
T
A
27
GENIC
possibly homozygous
52952801
8
32672362
32672363
G
A
12
GENIC
homozygous
52566452
8
32672458
32672494
TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
------------------------------------
4
GENIC
homozygous
53427450
8
32674269
32674270
C
T
31
GENIC
homozygous
52952803
8
32676065
32676066
C
T
34
GENIC
homozygous
52952805
8
32676172
32676173
A
G
17
GENIC
homozygous
52952807
8
32676312
32676313
T
C
21
GENIC
homozygous
52952813
8
32676460
32676461
C
T
20
GENIC
homozygous
52952815
8
32676732
32676733
T
C
30
GENIC
possibly homozygous
52566458
8
32676821
32676822
G
A
27
GENIC
homozygous
52952817
8
32676896
32676897
G
T
24
GENIC
possibly homozygous
53427452
8
32677114
32677117
TTT
---
24
GENIC
homozygous
52566467
8
32677373
32677374
A
T
15
GENIC
homozygous
52952819
8
32677668
32677669
G
GCTACTTTCT
26
GENIC
homozygous
52566473
