chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
119144577
119144578
A
G
24
GENIC
homozygous
115851174
7
119150645
119150646
A
G
25
GENIC
homozygous
115851176
7
119150999
119151000
C
T
35
GENIC
homozygous
115851178
7
119151113
119151114
A
T
34
GENIC
homozygous
115851180
7
119151266
119151267
T
C
33
GENIC
homozygous
115851182
7
119151512
119151513
T
A
25
GENIC
homozygous
115851184
7
119151622
119151623
C
T
23
GENIC
homozygous
115851186
7
119151904
119151980
TCTGAGAAGGCAGCCCTCTGACGGACGTGATGCCGGTGCATGCTTACAAGCACTGCACTTGGAGGGTGGCAGGGGA
10
GENIC
homozygous
128511279
7
119148191
119148195
TGGG
26
GENIC
homozygous
128511275
7
119149940
119149941
T
12
GENIC
possibly homozygous
128511277
7
119151130
119151130
C
29
GENIC
homozygous
128511278
7
119149170
119149171
A
C
9
GENIC
homozygous
129947080
7
119149170
119149170
C
9
GENIC
homozygous
129939139
7
119149944
119149945
T
G
11
GENIC
possibly homozygous
118259005
7
119149946
119149947
T
G
12
GENIC
possibly homozygous
118259007
7
119149948
119149949
T
G
11
GENIC
possibly homozygous
118259009
7
119152381
119152382
C
T
27
GENIC
homozygous
115851188
7
119152882
119152883
T
23
GENIC
homozygous
128511280
7
119153213
119153213
C
30
GENIC
homozygous
128511281
7
119153214
119153215
G
A
31
GENIC
homozygous
118259011
7
119153931
119153932
C
G
27
GENIC
homozygous
115851190
7
119153943
119153944
G
A
26
GENIC
homozygous
115851192
7
119154619
119154620
C
T
22
GENIC
homozygous
115851194
7
119154789
119154790
T
C
26
GENIC
homozygous
115851196
7
119154819
119154820
C
G
22
GENIC
homozygous
115851198
7
119155758
119155759
G
T
17
GENIC
homozygous
115851200
7
119156267
119156268
C
A
23
GENIC
homozygous
115851202
7
119156776
119156777
C
T
28
GENIC
homozygous
115851204
7
119156800
119156801
G
A
28
GENIC
homozygous
115851206
7
119156862
119156862
GA
35
GENIC
homozygous
128511282
7
119157193
119157194
T
C
29
GENIC
homozygous
115851208
7
119157837
119157838
A
G
23
GENIC
homozygous
115851210