chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
167181188
167181189
A
G
22
GENIC
homozygous
108357618
1
167184389
167184390
A
G
16
GENIC
homozygous
108357619
1
167186792
167186793
T
G
11
GENIC
homozygous
108357620
1
167187267
167187268
C
T
19
GENIC
homozygous
108357621
1
167189303
167189304
C
T
13
GENIC
homozygous
108357622
1
167189616
167189617
T
G
16
GENIC
homozygous
108357623
1
167189694
167189695
A
G
6
GENIC
homozygous
108357624
1
167190028
167190029
A
G
15
GENIC
homozygous
108357625
1
167190085
167190086
C
T
19
GENIC
homozygous
108357626
1
167190748
167190749
G
A
34
GENIC
homozygous
108357628
1
167191054
167191055
G
A
31
GENIC
homozygous
108357629
1
167191072
167191073
A
G
28
GENIC
homozygous
108357630
1
167192105
167192106
G
T
21
GENIC
homozygous
108357631
1
167189711
167189711
G
1
GENIC
homozygous
131780284
1
167187346
167187346
TTTGTTTG
16
GENIC
homozygous
127453808
1
167189707
167189708
T
1
GENIC
homozygous
127453809
1
167192439
167192503
GGTAGGCCTGAGAGTGGGTGGGCCTGAGAGTGGGAAGGCCTGAGAGTGGGAAGGCCTGAGAATA
20
GENIC
homozygous
127453810
1
167189713
167189714
T
G
1
GENIC
homozygous
120474500
