chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
130263548
130263678
AAAAATATTTAAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCTGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAACCAAAAAAAA
14
GENIC
homozygous
128520266
7
130263869
130263870
T
C
18
GENIC
homozygous
115889669
7
130264001
130264030
GGAGGACAGTCCTATGTGTATTGTGTGAG
16
GENIC
homozygous
128520267
7
130264554
130264555
C
T
25
GENIC
homozygous
115889677
7
130265055
130265056
T
C
29
GENIC
homozygous
115889679
7
130265966
130265981
AAAACAAAGTTGACT
19
GENIC
homozygous
128520268
7
130266609
130266610
T
C
33
GENIC
homozygous
115889681
7
130267073
130267074
A
T
26
GENIC
homozygous
115889683
7
130267182
130267183
G
C
27
GENIC
homozygous
115889685
7
130267217
130267218
C
T
24
GENIC
homozygous
115889687
7
130267486
130267487
A
C
29
GENIC
homozygous
115889689
7
130267498
130267499
T
C
25
GENIC
homozygous
115889692
7
130268656
130268657
C
T
21
GENIC
homozygous
115889694
7
130268681
130268682
T
C
19
GENIC
homozygous
115889696
7
130270754
130270755
T
C
37
GENIC
possibly homozygous
115889698
7
130271225
130271229
AGAT
36
GENIC
homozygous
128520269
7
130271482
130271482
A
33
GENIC
homozygous
128520270
7
130271916
130271917
T
C
28
GENIC
homozygous
115889700
7
130272607
130272608
T
C
39
GENIC
homozygous
115889702
7
130273416
130273417
G
A
38
GENIC
homozygous
115889704
7
130274101
130274102
A
G
33
GENIC
homozygous
115889706
7
130277368
130277377
AAGCAACAT
28
GENIC
homozygous
128520271
7
130284801
130284802
C
T
31
GENIC
homozygous
115889708
7
130285606
130285607
A
G
30
GENIC
homozygous
115889710
7
130286818
130286819
C
A
29
GENIC
homozygous
115889712
7
130287675
130287676
C
T
37
GENIC
homozygous
115889714