chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
130263548
130263678
AAAAATATTTAAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCTGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAACCAAAAAAAA
26
GENIC
possibly homozygous
128520266
7
130263869
130263870
T
C
52
GENIC
homozygous
115889669
7
130264142
130264170
TGAGGAAGACAGTCCTATGTGTGCTGTA
42
GENIC
homozygous
132658232
7
130264554
130264555
C
T
46
GENIC
homozygous
115889677
7
130264816
130264817
C
T
49
GENIC
homozygous
116229460
7
130265055
130265056
T
C
55
GENIC
homozygous
115889679
7
130266099
130266109
GCCCACAGGT
38
GENIC
homozygous
132658233
7
130266609
130266610
T
C
47
GENIC
homozygous
115889681
7
130267067
130267068
G
A
57
GENIC
homozygous
116229461
7
130267182
130267183
G
C
55
GENIC
homozygous
115889685
7
130267217
130267218
C
T
54
GENIC
homozygous
115889687
7
130267486
130267487
A
C
57
GENIC
homozygous
115889689
7
130268681
130268682
T
C
45
GENIC
homozygous
115889696
7
130268732
130268733
G
T
51
GENIC
homozygous
116229462
7
130268819
130268820
C
G
67
GENIC
homozygous
116229463
7
130270510
130270511
C
A
53
GENIC
homozygous
116346054
7
130271225
130271229
AGAT
49
GENIC
homozygous
128520269
7
130271916
130271917
T
C
46
GENIC
homozygous
115889700
7
130272607
130272608
T
C
48
GENIC
homozygous
115889702
7
130274101
130274102
A
G
45
GENIC
homozygous
115889706
7
130277250
130277251
C
T
73
GENIC
homozygous
116229465
7
130277368
130277377
AAGCAACAT
57
GENIC
homozygous
128520271
7
130283433
130283434
G
A
55
GENIC
homozygous
116229469
7
130285542
130285543
C
T
59
GENIC
homozygous
116229470
7
130286818
130286819
C
A
51
GENIC
homozygous
115889712