chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
5
60780790
60780795
GCTCG
52
GENIC
homozygous
141682657
5
60780824
60780825
A
G
62
GENIC
homozygous
141727800
5
60783677
60783678
C
T
61
GENIC
homozygous
141727806
5
60781216
60781217
G
C
49
GENIC
homozygous
146131338
5
60781586
60781587
A
T
35
GENIC
homozygous
141727801
5
60782150
60782151
T
A
52
GENIC
homozygous
141727802
5
60782340
60782341
T
G
59
GENIC
homozygous
141727803
5
60783318
60783319
A
G
47
GENIC
homozygous
141727805
5
60781464
60781465
C
14
GENIC
possibly homozygous
146120573
5
60783834
60783835
C
T
50
GENIC
homozygous
141727807
5
60784784
60784785
A
G
43
GENIC
homozygous
141727809
5
60784878
60784879
G
A
43
GENIC
homozygous
146131339
5
60785445
60785446
T
C
58
GENIC
homozygous
141727810
5
60786358
60786359
C
T
50
GENIC
homozygous
146131340
5
60786459
60786459
T
42
GENIC
homozygous
146120574
5
60786638
60786639
T
G
46
GENIC
homozygous
146131341
5
60786639
60786640
C
A
47
GENIC
homozygous
146131342
5
60787539
60787540
C
T
56
GENIC
homozygous
146131343
5
60787916
60787916
GGGT
28
GENIC
homozygous
141682658
5
60788568
60788569
A
T
45
GENIC
homozygous
146131344
5
60792123
60792124
T
C
68
GENIC
homozygous
137482132
5
60783135
60783135
T
53
GENIC
homozygous
137311563
5
60784989
60784999
GTGTGTGTGC
32
GENIC
heterozygous
147865970
5
60788014
60788015
C
T
57
GENIC
homozygous
137482127
5
60790159
60790160
A
C
40
GENIC
homozygous
137482129
5
60789064
60789076
TCCTCCTCTTCC
30
GENIC
homozygous
147664270
5
60789199
60789241
TCCTCCTCCTCTTCCTCCTCCTCTTCTTCCTCCTCCTCCTTT
35
GENIC
homozygous
147664271
5
60792551
60792552
T
G
63
GENIC
homozygous
137482133
5
60793229
60793230
T
C
56
GENIC
homozygous
137482134
5
60794213
60794214
G
T
53
GENIC
homozygous
146131345
5
60794742
60794743
C
T
68
GENIC
homozygous
146131346
5
60795230
60795231
C
T
52
GENIC
homozygous
146131347
5
60795864
60795865
C
T
53
GENIC
homozygous
146131348
5
60796889
60796890
A
G
44
GENIC
homozygous
137482136
5
60797214
60797215
A
G
55
GENIC
homozygous
137482137