chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
47319528
47319529
T
C
12
GENIC
homozygous
53181713
8
47319725
47319726
C
T
16
GENIC
homozygous
53109389
8
47319891
47319892
C
T
24
GENIC
homozygous
53181714
8
47319923
47319924
T
C
23
GENIC
homozygous
53181715
8
47319931
47319932
T
C
21
GENIC
homozygous
53109390
8
47319973
47319974
C
CAA
10
GENIC
heterozygous
53562918
8
47319974
47319975
A
-
10
GENIC
heterozygous
53562919
8
47320614
47320615
G
A
23
GENIC
homozygous
53181716
8
47320760
47320761
G
T
27
GENIC
possibly homozygous
53181717
8
47321519
47321526
GTGATAG
-------
18
GENIC
homozygous
53181718
8
47322027
47322028
T
TTCTGAAGGGGCTGCTCCCAGAGAAGAAATGAAA
35
GENIC
homozygous
53635724
8
47322274
47322275
C
T
15
GENIC
homozygous
53181722
8
47323092
47323093
T
C
23
GENIC
homozygous
53181723
8
47323572
47323573
G
A
19
GENIC
homozygous
53181724
8
47323584
47323585
C
T
21
GENIC
homozygous
53181725
8
47324461
47324462
C
T
21
GENIC
homozygous
53181726
8
47326295
47326296
C
T
22
GENIC
homozygous
53181727
8
47326975
47326976
A
G
7
GENIC
homozygous
53181728
8
47328395
47328396
A
G
21
GENIC
homozygous
53181729
8
47328677
47328678
A
G
32
GENIC
homozygous
53181730
8
47329489
47329490
T
C
12
GENIC
homozygous
53181731
8
47329935
47329936
G
A
15
GENIC
homozygous
53181732
8
47330150
47330151
T
A
29
GENIC
homozygous
53181733
8
47330294
47330295
A
G
17
GENIC
homozygous
53181734
8
47330705
47330706
C
CTTTTTTTTT
13
GENIC
homozygous
53460158
