chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
5
49255337
49255379
GATGGGGAGGATGAGTATAGAGAGGAGGATGATGGGGAGGGT
4
GENIC
homozygous
141001916
5
49255711
49255712
A
C
27
GENIC
homozygous
141003638
5
49255845
49255846
G
A
23
GENIC
homozygous
137459044
5
49255931
49255932
C
T
27
GENIC
homozygous
141003639
5
49256203
49256204
T
A
41
GENIC
homozygous
137459045
5
49256308
49256309
T
C
40
GENIC
homozygous
141003640
5
49256315
49256316
A
C
42
GENIC
homozygous
141003641
5
49256520
49256521
T
C
36
GENIC
homozygous
141003642
5
49256543
49256544
G
T
35
GENIC
homozygous
141003643
5
49257702
49257703
T
G
13
GENIC
homozygous
141003644
5
49257717
49257718
G
T
13
GENIC
homozygous
141003645
5
49257972
49257974
CA
34
GENIC
homozygous
141001917
5
49259919
49259951
CAGGATCACAGGATCTCAGGATCACAGGATCC
39
GENIC
homozygous
141001918
5
49261092
49261093
C
A
38
GENIC
homozygous
141003646
5
49261776
49261777
G
A
37
GENIC
homozygous
141003647
5
49262087
49262088
C
T
45
GENIC
homozygous
141003648
5
49262353
49262354
C
T
50
GENIC
homozygous
137459052
5
49271219
49271220
T
C
38
GENIC
homozygous
141003649
5
49272170
49272171
C
13
GENIC
possibly homozygous
141001919
5
49273927
49273928
G
C
30
GENIC
homozygous
141003650
5
49274307
49274308
C
T
38
GENIC
homozygous
141003651
5
49274349
49274350
C
G
35
GENIC
homozygous
141003652
5
49274638
49274639
T
C
34
GENIC
homozygous
141003653
5
49276276
49276281
CTTAA
30
GENIC
homozygous
141001920
5
49278482
49278483
T
C
44
GENIC
homozygous
141003654
5
49279285
49279286
T
A
41
GENIC
homozygous
141003655
5
49279374
49279375
G
T
43
GENIC
possibly homozygous
141003656
5
49283468
49283469
A
G
47
GENIC
homozygous
141003659
5
49279919
49279920
A
G
39
GENIC
homozygous
141003657
5
49281343
49281344
C
T
40
GENIC
homozygous
141003658
5
49282627
49282628
A
C
37
GENIC
homozygous
137459059
5
49284994
49284995
T
C
53
GENIC
homozygous
137459061
5
49285295
49285296
A
G
57
GENIC
homozygous
141003660