chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
47319528
47319529
T
C
13
GENIC
homozygous
53181713
8
47319725
47319726
C
T
19
GENIC
possibly homozygous
53109389
8
47319891
47319892
C
T
11
GENIC
possibly homozygous
53181714
8
47320614
47320615
G
A
23
GENIC
possibly homozygous
53181716
8
47320760
47320761
G
T
9
GENIC
homozygous
53181717
8
47321519
47321526
GTGATAG
-------
5
GENIC
homozygous
53181718
8
47321781
47321782
G
T
18
GENIC
possibly homozygous
54092823
8
47322027
47322028
T
TTCTGAAGGGGCTGCTCCCAGAGAAGAAATGAAA
2
GENIC
heterozygous
53635724
8
47322392
47322393
A
-
2
GENIC
heterozygous
53610824
8
47323092
47323093
T
C
15
GENIC
possibly homozygous
53181723
8
47323572
47323573
G
A
12
GENIC
homozygous
53181724
8
47323888
47323889
G
A
13
GENIC
heterozygous
54092825
8
47324461
47324462
C
T
25
GENIC
homozygous
53181726
8
47325574
47325575
G
T
8
GENIC
heterozygous
54092827
8
47325575
47325576
C
T
8
GENIC
heterozygous
54092829
8
47325997
47325998
G
C
16
GENIC
heterozygous
54092831
8
47326975
47326976
A
G
14
GENIC
homozygous
53181728
8
47328395
47328396
A
G
24
GENIC
possibly homozygous
53181729
8
47328677
47328678
A
G
25
GENIC
homozygous
53181730
8
47329489
47329490
T
C
15
GENIC
homozygous
53181731
8
47330150
47330151
T
A
11
GENIC
homozygous
53181733
8
47330167
47330171
CTGT
----
9
GENIC
homozygous
54092833
8
47330294
47330295
A
G
14
GENIC
homozygous
53181734
