chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
32666616
32666617
G
A
28
GENIC
homozygous
52566406
8
32667177
32667178
G
A
14
GENIC
homozygous
52566410
8
32667222
32667223
T
C
12
GENIC
homozygous
52566413
8
32667363
32667364
C
G
24
GENIC
homozygous
52566416
8
32667456
32667457
T
C
27
GENIC
homozygous
52566422
8
32667527
32667528
T
-
18
GENIC
homozygous
52566425
8
32668262
32668263
T
TA
7
GENIC
homozygous
52566428
8
32668298
32668299
C
CTTTTTTTTTTT
8
GENIC
heterozygous
53375617
8
32668757
32668758
A
AG
22
GENIC
homozygous
52952791
8
32669348
32669349
G
C
21
GENIC
homozygous
52952793
8
32669504
32669505
C
T
28
GENIC
possibly homozygous
53098180
8
32669793
32669809
CAACCAACCAAACAAA
----------------
14
GENIC
homozygous
53375618
8
32670119
32670121
AA
--
11
GENIC
homozygous
52952797
8
32670406
32670407
C
CTTTTTTTTTTTTTTTTT
7
GENIC
heterozygous
53375619
8
32670453
32670454
A
-
9
GENIC
homozygous
53098182
8
32671756
32671757
T
A
27
GENIC
homozygous
52952801
8
32671878
32671879
G
A
23
GENIC
homozygous
53098183
8
32672214
32672215
C
G
21
GENIC
homozygous
53098184
8
32672362
32672363
G
A
13
GENIC
homozygous
52566452
8
32672422
32672423
C
T
14
GENIC
homozygous
53098186
8
32672458
32672496
TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
--------------------------------------
2
GENIC
homozygous
53375620
8
32676065
32676066
C
T
23
GENIC
homozygous
52952805
8
32676172
32676173
A
G
11
GENIC
homozygous
52952807
8
32676190
32676191
C
CAA
11
GENIC
heterozygous
52952809
8
32676190
32676191
C
CA
11
GENIC
heterozygous
52952811
8
32676312
32676313
T
C
25
GENIC
homozygous
52952813
8
32676732
32676733
T
C
18
GENIC
homozygous
52566458
8
32676821
32676822
G
A
12
GENIC
homozygous
52952817
8
32676896
32676897
G
-
4
GENIC
homozygous
52566464
8
32677114
32677117
TTT
---
9
GENIC
homozygous
52566467
8
32677373
32677374
A
T
9
GENIC
homozygous
52952819
8
32677374
32677375
A
T
9
GENIC
homozygous
53375621
8
32677668
32677669
G
GCTACTTTCT
23
GENIC
homozygous
52566473
