chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
59595061
59595062
T
C
27
GENIC
homozygous
52664068
8
59596396
59596397
T
G
21
GENIC
homozygous
52983288
8
59596828
59596829
T
C
10
GENIC
homozygous
53388675
8
59596830
59596831
C
CAGTT
10
GENIC
homozygous
53388676
8
59596833
59596834
T
TAGAGCGC
11
GENIC
homozygous
53388677
8
59596835
59596836
T
TGC
11
GENIC
homozygous
53388678
8
59596999
59597058
TATTATAGGAAATAGATAATTTTACTTTTTCCTCTCCAGCTTGGATCAATTTTATTTAC
-----------------------------------------------------------
6
GENIC
homozygous
53388679
8
59597350
59597351
C
T
21
GENIC
homozygous
52983290
8
59597430
59597431
C
CAA
5
GENIC
homozygous
52664080
8
59598668
59598669
A
-
16
GENIC
homozygous
52983292
8
59603281
59603282
A
G
23
GENIC
homozygous
52664084
8
59603988
59603989
T
C
27
GENIC
homozygous
52664086
8
59604976
59604977
G
GAAAAAAAA
3
GENIC
heterozygous
53388680
8
59605092
59605093
T
-
7
GENIC
homozygous
52664090
8
59605240
59605241
T
-
16
GENIC
homozygous
53364020
8
59607059
59607060
C
T
31
GENIC
homozygous
52983293