chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
85979308
85979309
T
C
43
GENIC
possibly homozygous
142842935
1
85979824
85979825
A
G
44
GENIC
homozygous
142842936
1
85984013
85984014
C
T
43
GENIC
homozygous
142842937
1
85984018
85984019
C
T
44
GENIC
homozygous
142842938
1
85984875
85984876
T
C
44
GENIC
homozygous
142842939
1
85985020
85985021
T
C
48
GENIC
homozygous
142842940
1
85986122
85986123
T
A
25
GENIC
homozygous
142842941
1
85986132
85986133
G
A
24
GENIC
homozygous
142842942
1
85986183
85986184
G
A
27
GENIC
homozygous
142842943
1
85986537
85986538
G
A
38
GENIC
homozygous
142842944
1
85986783
85986784
C
T
34
GENIC
homozygous
142842945
1
85987345
85987346
T
G
19
GENIC
homozygous
142842946
1
85987807
85987808
C
T
22
GENIC
homozygous
142842947
1
85988242
85988243
G
C
44
GENIC
homozygous
142842948
1
85988422
85988423
G
A
33
GENIC
homozygous
142842949
1
85988777
85988778
G
A
39
GENIC
homozygous
142842950
1
85988840
85988841
A
G
42
GENIC
homozygous
142842951
1
85988868
85988869
T
C
39
GENIC
homozygous
142842952
1
85979905
85979905
CCTGTACCTGATGTACCTGCAAGTTCCCTGTGCATCTG
37
GENIC
homozygous
142790330
1
85979909
85979909
CG
35
GENIC
homozygous
142790331
1
85986182
85986182
T
27
GENIC
homozygous
142790332
1
85987167
85987167
GTGTGTGTGTGC
15
GENIC
homozygous
142790333
1
85987925
85987925
AG
26
GENIC
homozygous
142790334
1
85989747
85989771
CTGCTGCAGCTGCCTCCGTCAGAC
28
GENIC
homozygous
142790335
1
85980348
85980363
TTCTTTCTTTCTTTC
33
GENIC
possibly homozygous
146588436
1
85987277
85987277
ATG
14
GENIC
homozygous
143740130
1
85987278
85987278
A
13
GENIC
homozygous
143740131
1
85991126
85991126
TG
42
GENIC
possibly homozygous
142790336
1
85991228
85991229
T
C
28
GENIC
homozygous
143785779
1
85980306
85980307
C
39
GENIC
heterozygous
402951676
1
85980306
85980307
C
T
39
GENIC
homozygous
402951677
1
85991515
85991516
T
A
44
GENIC
homozygous
142842953
1
85993293
85993294
C
G
48
GENIC
possibly homozygous
142842954
1
85991230
85991231
T
C
28
GENIC
homozygous
143785780
