chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
110725452
110725453
G
A
46
GENIC
homozygous
138181611
7
110726144
110726145
T
C
44
GENIC
homozygous
138181612
7
110727712
110727713
C
T
34
GENIC
homozygous
138181614
7
110727810
110727811
A
G
35
GENIC
homozygous
138181615
7
110727916
110727917
A
G
37
GENIC
homozygous
138181616
7
110728499
110728500
A
G
39
GENIC
homozygous
138181617
7
110728591
110728592
G
C
36
GENIC
homozygous
138181619
7
110729130
110729131
T
C
48
GENIC
homozygous
138181621
7
110729373
110729374
A
G
48
GENIC
homozygous
138181622
7
110729983
110729984
A
G
50
GENIC
homozygous
138181623
7
110730425
110730426
G
A
38
GENIC
homozygous
138181624
7
110731139
110731140
G
A
39
GENIC
homozygous
143365413
7
110731952
110731953
T
C
58
GENIC
homozygous
138181626
7
110733000
110733001
T
C
40
GENIC
homozygous
138181627
7
110733126
110733127
T
C
51
GENIC
homozygous
138181628
7
110733147
110733148
T
G
48
GENIC
homozygous
138181629
7
110733644
110733645
T
C
53
GENIC
homozygous
138181630
7
110734150
110734151
T
20
GENIC
homozygous
403617303
7
110734150
110734151
T
G
20
GENIC
heterozygous
403617304
7
110732886
110732886
CAGCTAGAC
43
GENIC
homozygous
137974146
7
110733164
110733279
CCTAAATCTGTCTTCTTTTTTGGTTCTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCCT
42
GENIC
possibly homozygous
137974147
