chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
116687137
116687138
A
G
60
GENIC
possibly homozygous
116669925
8
116687145
116687146
A
C
62
GENIC
possibly homozygous
116669927
8
116687608
116687609
T
A
62
GENIC
possibly homozygous
117149181
8
116689561
116689562
A
G
50
GENIC
homozygous
116669929
8
116689917
116689918
G
A
52
GENIC
homozygous
117149182
8
116690826
116690827
G
T
48
GENIC
possibly homozygous
116669931
8
116690942
116690943
T
C
38
GENIC
homozygous
117149184
8
116690968
116690969
A
G
32
GENIC
homozygous
117149185
8
116690970
116690971
A
G
32
GENIC
homozygous
117149186
8
116691400
116691401
C
G
36
GENIC
homozygous
117149187
8
116692292
116692293
T
G
45
GENIC
homozygous
117149188
8
116693665
116693666
T
C
41
GENIC
homozygous
117149189
8
116693668
116693669
G
A
42
GENIC
homozygous
117149190
8
116694075
116694075
CA
52
GENIC
homozygous
128635194
8
116689660
116689663
TCT
22
GENIC
possibly homozygous
128635192
8
116690882
116690882
TGTTGT
37
GENIC
homozygous
128635193
8
116689857
116689858
T
C
51
GENIC
possibly homozygous
116886639
8
116696917
116696918
T
C
62
GENIC
homozygous
117149191
8
116699218
116699219
A
G
60
GENIC
homozygous
116669937
8
116699286
116699287
C
T
53
GENIC
homozygous
117149192
8
116699482
116699483
C
T
59
GENIC
homozygous
117149193
8
116695805
116695921
TGAACTACTTGCTAAGGCTGGGGATTTAGCTTAGTGGTAGAGCACTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCTGAAAAAAAAAAAAAAAAAAACCATTCCTC
21
GENIC
possibly homozygous
131054199