chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
89180275
89180276
T
C
32
GENIC
homozygous
108884780
1
89180560
89180561
C
G
34
GENIC
homozygous
108884781
1
89180810
89180811
G
A
34
GENIC
homozygous
120780190
1
89185838
89185839
T
C
22
GENIC
homozygous
108884792
1
89185983
89185984
T
C
33
GENIC
homozygous
108884793
1
89186433
89186434
C
T
37
GENIC
homozygous
108884794
1
89180870
89180870
CACCTGTACCTGATGTACCTGCAAGTTCCCTGTGCATCTG
37
GENIC
homozygous
127402171
1
89187085
89187086
T
A
26
GENIC
homozygous
120483939
1
89187146
89187147
G
A
25
GENIC
homozygous
120483941
1
89187220
89187221
A
C
16
GENIC
homozygous
108884795
1
89187270
89187271
A
G
15
GENIC
homozygous
108884796
1
89187500
89187501
G
A
20
GENIC
homozygous
108884797
1
89187746
89187747
C
T
20
GENIC
homozygous
109308026
1
89188308
89188309
T
G
18
GENIC
homozygous
108884798
1
89188565
89188566
C
T
20
GENIC
homozygous
120780191
1
89189204
89189205
G
C
21
GENIC
homozygous
108884800
1
89189802
89189803
A
G
20
GENIC
homozygous
108884802
1
89192088
89192088
TG
32
GENIC
homozygous
131260010
1
89192205
89192206
G
T
24
GENIC
homozygous
134180452
1
89189751
89189752
C
T
16
GENIC
homozygous
134180447
1
89189774
89189775
T
A
19
GENIC
homozygous
134180448
1
89192184
89192185
C
T
19
GENIC
homozygous
134180449
1
89192186
89192187
C
T
20
GENIC
homozygous
134180450
1
89192188
89192189
C
T
20
GENIC
homozygous
134180451
1
89192116
89192116
ATAG
15
GENIC
heterozygous
134171134
1
89192196
89192198
CA
20
GENIC
homozygous
134171135
1
89192477
89192478
T
A
28
GENIC
homozygous
108884806
1
89192937
89192938
T
G
19
GENIC
homozygous
120780192
1
89193568
89193569
C
A
25
GENIC
homozygous
120780193
1
89194190
89194191
C
T
23
GENIC
possibly homozygous
134180453
