chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
128028359
128028360
T
C
20
GENIC
homozygous
52884672
8
128028481
128028482
C
CTTTTA
10
GENIC
homozygous
52884673
8
128029480
128029481
C
CACTTAGGATCTGAGTCCCTTCAAGAAGACTTAGTTCCCGCATAAGGCGACTA
34
GENIC
heterozygous
53415171
8
128029653
128029654
C
CTT
18
GENIC
possibly homozygous
52884674
8
128030090
128030091
T
C
29
GENIC
homozygous
52884678
8
128030446
128030447
T
C
36
GENIC
homozygous
52884679
8
128031132
128031133
G
A
24
GENIC
homozygous
52884680
8
128031353
128031354
C
T
28
GENIC
homozygous
52884681
8
128031364
128031365
C
T
30
GENIC
homozygous
52884682
8
128032203
128032204
G
A
18
GENIC
homozygous
52884683
8
128032444
128032445
T
C
29
GENIC
homozygous
52884684
8
128032721
128032722
A
AACACAC
10
GENIC
homozygous
53415172
8
128033460
128033461
A
G
26
GENIC
homozygous
52884686
8
128033467
128033468
T
A
26
GENIC
homozygous
52884687
8
128033793
128033835
CCCGCCCCTTCCCGCCCCGTGCCCGCCCCTGCAGGCCTGTGT
------------------------------------------
2
GENIC
homozygous
53415173
8
128034345
128034346
A
AT
25
GENIC
homozygous
52884688
8
128034346
128034347
A
T
25
GENIC
homozygous
53064453
8
128034695
128034696
C
-
3
GENIC
homozygous
52884691
8
128034697
128034699
TA
--
3
GENIC
homozygous
52884693
8
128035400
128035401
A
AC
21
GENIC
homozygous
52884694
8
128035410
128035411
C
CA
20
GENIC
homozygous
52884695
8
128035473
128035474
G
A
21
GENIC
homozygous
52884696
8
128035655
128035656
T
TGG
21
GENIC
possibly homozygous
52884697
8
128035655
128035656
T
TGGG
21
GENIC
heterozygous
53233205
