chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
86649542
86649543
T
C
67
GENIC
possibly homozygous
57527545
3
86650158
86650159
T
G
57
GENIC
homozygous
57527547
3
86650446
86650447
A
G
58
GENIC
homozygous
57527549
3
86651965
86651998
GCAGGCTTTGCCATGCCCATTCTCTCTAGAAAT
---------------------------------
14
GENIC
homozygous
57527555
3
86651969
86651970
G
GGC
18
GENIC
heterozygous
57527557
3
86651974
86651975
G
-
11
GENIC
homozygous
57527559
3
86652641
86652642
A
G
53
GENIC
homozygous
57527563
3
86652700
86652701
A
G
45
GENIC
homozygous
57527565
3
86653463
86653464
C
T
43
GENIC
possibly homozygous
57922200
3
86653530
86653531
A
AG
27
GENIC
homozygous
57527571
3
86654204
86654205
T
C
58
GENIC
homozygous
57527575
3
86655312
86655313
T
-
11
GENIC
heterozygous
57527577
3
86657065
86657066
C
T
54
GENIC
possibly homozygous
57922202
3
86657171
86657172
T
TGTGC
27
GENIC
homozygous
57527581
3
86657541
86657542
C
T
68
GENIC
possibly homozygous
57922204
3
86657553
86657554
C
T
59
GENIC
possibly homozygous
57527583
3
86657749
86657750
T
TTCC
39
GENIC
homozygous
57527585
3
86658265
86658268
TCC
---
10
GENIC
homozygous
57527589
3
86658277
86658278
T
-
12
GENIC
heterozygous
57527591
3
86659886
86659887
G
C
63
GENIC
homozygous
57527597
3
86659987
86659988
A
G
44
GENIC
possibly homozygous
57527599
3
86659992
86659993
G
A
44
GENIC
homozygous
57527601
3
86660136
86660137
T
C
62
GENIC
homozygous
57527603
3
86660639
86660640
T
C
30
GENIC
possibly homozygous
57922206
3
86660775
86660776
G
A
56
GENIC
homozygous
57527607
3
86661046
86661049
AAA
---
53
GENIC
homozygous
57527611
3
86661398
86661399
C
T
54
GENIC
homozygous
57527613
3
86662301
86662303
GG
--
38
GENIC
homozygous
57527617
3
86663019
86663020
T
G
53
GENIC
possibly homozygous
57922208
3
86664060
86664061
A
AAGACG
30
GENIC
homozygous
57527625
3
86664073
86664074
C
A
44
GENIC
heterozygous
57922210