chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
89180275
89180276
T
C
43
GENIC
possibly homozygous
108884780
1
89180791
89180792
A
G
64
GENIC
homozygous
108884782
1
89184976
89184977
C
T
57
GENIC
homozygous
108884789
1
89185838
89185839
T
C
69
GENIC
possibly homozygous
108884792
1
89185983
89185984
T
C
56
GENIC
homozygous
108884793
1
89187146
89187147
G
A
37
GENIC
homozygous
120483941
1
89180872
89180872
CCTGTACCTGATGTACCTGCAAGTTCCCTGTGCATCTG
54
GENIC
homozygous
131260003
1
89180876
89180876
CG
54
GENIC
homozygous
131260004
1
89187145
89187145
T
38
GENIC
homozygous
131260006
1
89187085
89187086
T
A
41
GENIC
homozygous
120483939
1
89187095
89187096
G
A
42
GENIC
homozygous
120483940
1
89184981
89184982
C
T
56
GENIC
homozygous
120503177
1
89187270
89187271
A
G
42
GENIC
homozygous
108884796
1
89187500
89187501
G
A
43
GENIC
homozygous
108884797
1
89187746
89187747
C
T
40
GENIC
homozygous
109308026
1
89188240
89188240
ATG
20
GENIC
homozygous
131576398
1
89188241
89188241
A
20
GENIC
homozygous
131576399
1
89188308
89188309
T
G
37
GENIC
homozygous
108884798
1
89188769
89188770
C
T
23
GENIC
homozygous
108884799
1
89188887
89188887
AG
51
GENIC
homozygous
131260008
1
89189204
89189205
G
C
53
GENIC
homozygous
108884800
1
89189384
89189385
G
A
46
GENIC
homozygous
108884801
1
89189802
89189803
A
G
43
GENIC
homozygous
108884802
1
89189830
89189831
T
C
43
GENIC
homozygous
108884803
1
89190709
89190733
CTGCTGCAGCTGCCTCCGTCAGAC
40
GENIC
homozygous
131260009
1
89192088
89192088
TG
32
GENIC
homozygous
131260010
1
89192190
89192191
T
C
30
GENIC
homozygous
109308036
1
89192477
89192478
T
A
50
GENIC
homozygous
108884806
1
89194255
89194256
C
G
60
GENIC
possibly homozygous
125397014
1
89189739
89189740
G
A
45
GENIC
possibly homozygous
131276989
1
89192192
89192193
T
C
30
GENIC
homozygous
131593207
