chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
14
94422413
94422414
T
A
66
GENIC
homozygous
139594749
14
94428690
94428704
CATGTGTATTGGTA
46
GENIC
homozygous
139410748
14
94428721
94428722
A
T
50
GENIC
possibly homozygous
139594750
14
94428831
94428832
A
G
52
GENIC
possibly homozygous
139594751
14
94429052
94429053
A
G
50
GENIC
homozygous
139594752
14
94429234
94429235
T
C
37
GENIC
possibly homozygous
139594753
14
94429302
94429303
G
A
55
GENIC
homozygous
139594754
14
94429309
94429310
G
A
55
GENIC
homozygous
139594755
14
94429321
94429321
CC
57
GENIC
homozygous
139410749
14
94429324
94429325
C
T
57
GENIC
homozygous
139594756
14
94429438
94429439
A
G
50
GENIC
homozygous
139594757
14
94429461
94429462
A
G
48
GENIC
homozygous
139594758
14
94429651
94429652
G
48
GENIC
homozygous
139410750
14
94429984
94429984
GCTGC
27
GENIC
homozygous
139410751
14
94430498
94430502
CTTC
19
GENIC
homozygous
139410752
14
94430747
94430748
G
A
56
GENIC
homozygous
139594759
14
94432780
94432781
C
T
29
GENIC
homozygous
139594760
14
94434767
94434768
G
A
61
GENIC
homozygous
139594761
14
94429507
94429508
T
C
53
GENIC
heterozygous
403366439
14
94429507
94429508
T
G
53
GENIC
possibly homozygous
154867591
14
94437117
94437118
G
30
GENIC
homozygous
403655678
14
94437117
94437118
G
T
30
GENIC
heterozygous
403655679
14
94438565
94438566
A
C
43
GENIC
homozygous
139594762
14
94438881
94438922
CTCCTGAGTGCAGGAGTAAAAGTGTGCGCCACCACGAACAA
42
GENIC
homozygous
139410754
14
94439532
94439532
A
36
GENIC
heterozygous
139410755
14
94441171
94441172
T
C
46
GENIC
homozygous
139594763
14
94442709
94442710
G
A
22
GENIC
homozygous
139594764
14
94443698
94443699
A
T
59
GENIC
homozygous
139594765
14
94443742
94443743
G
A
55
GENIC
possibly homozygous
139594766
14
94444062
94444063
G
A
60
GENIC
possibly homozygous
139594767
14
94445104
94445105
A
G
70
GENIC
homozygous
139594768
14
94446528
94446529
A
T
65
GENIC
homozygous
139594769
