chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
109955603
109955604
A
C
30
GENIC
homozygous
138180209
7
109955853
109955853
GTGCTTCTCGGAA
16
GENIC
homozygous
137973835
7
109955961
109955962
T
C
14
GENIC
homozygous
138180210
7
109956421
109956422
T
C
12
GENIC
homozygous
138180211
7
109956658
109956659
A
G
20
GENIC
homozygous
138180212
7
109956725
109956726
C
A
22
GENIC
homozygous
138180213
7
109956771
109956772
C
G
18
GENIC
homozygous
138180214
7
109956879
109956880
T
C
26
GENIC
homozygous
138180215
7
109956912
109956913
G
A
27
GENIC
homozygous
138180216
7
109956961
109956968
GACCTCA
24
GENIC
homozygous
137973836
7
109956990
109956991
A
G
27
GENIC
homozygous
138180217
7
109957076
109957077
A
G
19
GENIC
homozygous
138180218
7
109957102
109957103
G
A
13
GENIC
homozygous
138180219
7
109957130
109957130
TT
11
GENIC
homozygous
137973837
7
109957136
109957136
AAGATTTATTTTATTTATTATATATAAGTATGCTGTAGCTGTCTTCAGACACACCAGTAGAGAGC
12
GENIC
possibly homozygous
137973838
7
109957196
109957197
A
G
12
GENIC
homozygous
138180220
7
109957490
109957491
C
T
20
GENIC
homozygous
138180221
7
109957587
109957588
T
C
18
GENIC
homozygous
138180222
7
109957663
109957663
TTTTGAGACGG
20
GENIC
homozygous
137973839
7
109957717
109957718
C
T
14
GENIC
homozygous
138180223
7
109957900
109957901
A
G
25
GENIC
homozygous
138180224
7
109958133
109958137
CTCT
24
GENIC
homozygous
137973840
7
109958743
109958744
T
C
24
GENIC
homozygous
138180225
7
109959462
109959463
C
G
26
GENIC
homozygous
138180226
7
109960043
109960044
T
C
20
GENIC
homozygous
138180227
7
109960476
109960477
C
T
18
GENIC
homozygous
138180228
7
109961575
109961576
G
A
16
GENIC
homozygous
138180229
7
109961899
109961899
C
25
GENIC
homozygous
137973841
7
109961940
109961941
A
G
26
GENIC
homozygous
138180230
7
109957612
109957613
A
13
GENIC
homozygous
403222113
7
109957612
109957613
A
T
13
GENIC
heterozygous
154488287
