chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
59595061
59595062
T
C
23
GENIC
homozygous
52664068
8
59596828
59596829
T
C
8
GENIC
homozygous
53388675
8
59596830
59596831
C
CAGTT
7
GENIC
homozygous
53388676
8
59596833
59596834
T
TAGAGCGC
6
GENIC
homozygous
53388677
8
59596835
59596836
T
TGC
6
GENIC
homozygous
53388678
8
59596874
59596875
G
GA
4
GENIC
heterozygous
53433223
8
59596999
59597058
TATTATAGGAAATAGATAATTTTACTTTTTCCTCTCCAGCTTGGATCAATTTTATTTAC
-----------------------------------------------------------
4
GENIC
homozygous
53388679
8
59597430
59597431
C
CAA
16
GENIC
heterozygous
52664080
8
59597430
59597431
C
CA
16
GENIC
possibly homozygous
52664082
8
59603281
59603282
A
G
26
GENIC
homozygous
52664084
8
59603988
59603989
T
C
41
GENIC
homozygous
52664086
8
59604957
59604958
C
CACCCTTGCCGCTTCACTTCTTGAGAACGCGCGCGCACGCGCGCTCTCACCAA
18
GENIC
heterozygous
53570150
8
59604976
59604977
G
GAAAAAAAA
7
GENIC
heterozygous
53388680
8
59604977
59604978
A
-
7
GENIC
possibly homozygous
52664088
8
59605092
59605093
T
-
12
GENIC
possibly homozygous
52664090
8
59605240
59605241
T
-
13
GENIC
homozygous
53364020
8
59605922
59605923
G
A
13
GENIC
homozygous
52664094
8
59606599
59606600
A
AAAAC
22
GENIC
homozygous
52664096
