chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
211206491
211206492
A
G
43
GENIC
homozygous
108523144
1
211206769
211206769
A
30
GENIC
homozygous
127479490
1
211207312
211207313
G
C
55
GENIC
homozygous
109448535
1
211207575
211207576
T
A
60
GENIC
homozygous
108523146
1
211208010
211208011
G
A
66
GENIC
homozygous
108523147
1
211211682
211211683
C
T
63
GENIC
homozygous
109448536
1
211213156
211213157
A
G
67
GENIC
possibly homozygous
108523162
1
211213288
211213289
A
G
63
GENIC
homozygous
109448537
1
211214667
211214668
G
T
61
GENIC
homozygous
108523166
1
211215409
211215410
G
A
56
GENIC
homozygous
108523169
1
211216139
211216140
T
C
55
GENIC
homozygous
108523171
1
211219571
211219571
T
42
GENIC
possibly homozygous
131582558
1
211213512
211213512
CATACTGCTCTTTTTATGTAAGTTCACGGTACACTGAAAGATCGGGTTCCATCACAGATGGTCATGAGCCACCATGTGGTTG
17
GENIC
homozygous
131582556
1
211214169
211214175
TTGTTG
49
GENIC
homozygous
131582557
1
211220653
211220654
A
G
60
GENIC
homozygous
109448538
1
211224654
211224655
C
A
59
GENIC
possibly homozygous
109448539
1
211225925
211225926
C
T
61
GENIC
homozygous
109448540
1
211227495
211227496
G
A
72
GENIC
homozygous
109448541
1
211235329
211235330
G
T
45
GENIC
homozygous
108523220
1
211237783
211237784
A
G
52
GENIC
homozygous
109448542
1
211239132
211239133
C
G
68
GENIC
homozygous
108523240