chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
29940338
29940339
T
C
55
GENIC
homozygous
138049624
7
29940434
29940435
T
C
52
GENIC
homozygous
144021156
7
29941656
29941657
C
T
47
GENIC
homozygous
144021157
7
29942225
29942226
C
T
60
GENIC
homozygous
144021158
7
29942288
29942289
A
G
53
GENIC
homozygous
144021159
7
29942710
29942711
G
A
63
GENIC
homozygous
144021160
7
29943431
29943432
A
C
41
GENIC
homozygous
138049626
7
29943522
29943523
G
C
38
GENIC
homozygous
138049627
7
29944295
29944296
C
T
36
GENIC
homozygous
144021161
7
29944922
29944923
A
C
44
GENIC
homozygous
144021162
7
29945167
29945168
A
G
40
GENIC
homozygous
138049628
7
29945717
29945718
T
A
56
GENIC
homozygous
138049631
7
29946195
29946196
A
G
41
GENIC
homozygous
138049632
7
29947930
29947931
T
C
54
GENIC
homozygous
138049633
7
29948115
29948117
TG
58
GENIC
homozygous
141909822
7
29948517
29948518
T
G
44
GENIC
homozygous
141949120
7
29940575
29940576
T
A
65
GENIC
homozygous
141949116
7
29946796
29946797
A
G
46
GENIC
homozygous
141949119
7
29943915
29943915
T
49
GENIC
homozygous
144003236
7
29948631
29948632
C
G
36
GENIC
homozygous
141949121
7
29948757
29948757
AGCGCTCTACCACTGAGCTAAATCCCCAGCC
42
GENIC
homozygous
137944705
7
29950501
29950501
AT
38
GENIC
homozygous
137944706
7
29951274
29951275
G
T
19
GENIC
heterozygous
403206138
7
29944671
29944672
A
35
GENIC
possibly homozygous
403206135
7
29944671
29944672
A
C
35
GENIC
heterozygous
403206136
7
29951274
29951275
G
19
GENIC
homozygous
403206137
7
29951281
29951282
G
T
15
GENIC
heterozygous
154433908
7
29951281
29951282
G
15
GENIC
possibly homozygous
403206139
7
29951941
29951942
A
G
49
GENIC
possibly homozygous
138049636
