chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
13
102638068
102638069
C
T
47
GENIC
homozygous
114586924
13
102638948
102638949
C
A
30
GENIC
homozygous
114694049
13
102638969
102638970
A
G
30
GENIC
homozygous
114694050
13
102639226
102639227
C
T
8
GENIC
possibly homozygous
118507081
13
102639255
102639256
T
C
10
GENIC
heterozygous
118529560
13
102639837
102639838
G
A
23
GENIC
homozygous
114694051
13
102640056
102640056
AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA
2
GENIC
homozygous
132714872
13
102639255
102639255
C
14
GENIC
heterozygous
132714869
13
102639640
102639641
G
10
GENIC
homozygous
132714870
13
102639868
102639868
A
21
GENIC
homozygous
132714871
13
102640101
102640102
G
A
8
GENIC
homozygous
118529561
13
102640181
102640181
T
31
GENIC
homozygous
132714873
13
102640593
102640594
T
C
27
GENIC
homozygous
114586932
13
102640724
102640725
G
A
36
GENIC
homozygous
114586934
13
102642306
102642307
A
42
GENIC
homozygous
132714874
13
102642362
102642363
A
T
45
GENIC
homozygous
114586938
13
102642450
102642451
G
C
40
GENIC
homozygous
114586940
13
102642611
102642612
C
T
25
GENIC
homozygous
114694052
13
102642790
102642791
T
G
37
GENIC
homozygous
114694053
