chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
20
5388821
5388822
A
G
14
GENIC
homozygous
45386510
20
5389655
5389656
G
A
8
GENIC
homozygous
45386519
20
5389773
5389774
C
G
20
GENIC
homozygous
45386521
20
5390225
5390226
T
TGGTCTCCCTGCCTACAGTTGTGGCCCCA
25
GENIC
homozygous
45818522
20
5390392
5390393
C
CACTTTCTTTCTGTCCGAGTAAGACACCTGCACAG
21
GENIC
homozygous
45862082
20
5391305
5391306
T
C
33
GENIC
homozygous
45386536
20
5391411
5391412
C
T
22
GENIC
homozygous
45731706
20
5391604
5391605
C
-
28
GENIC
homozygous
45731707
20
5391828
5391829
T
C
20
GENIC
homozygous
45731708
20
5391836
5391837
A
G
18
GENIC
homozygous
45386542
20
5392767
5392768
C
A
27
GENIC
homozygous
45386547
20
5394055
5394056
G
A
15
GENIC
homozygous
45752707
20
5394467
5394472
ACACA
-----
9
GENIC
homozygous
45731710
20
5394476
5394477
T
-
7
GENIC
homozygous
45386559
20
5394479
5394480
T
C
5
GENIC
homozygous
45862083
20
5394509
5394510
A
AC
3
GENIC
homozygous
45862084
20
5394512
5394513
C
CA
4
GENIC
heterozygous
45862085
20
5394516
5394517
A
AC
3
GENIC
homozygous
45862086
20
5395187
5395188
A
-
17
GENIC
homozygous
45752710
20
5395331
5395332
T
A
23
GENIC
homozygous
45386561
20
5395782
5395783
G
A
25
GENIC
homozygous
45386563
20
5395949
5395950
A
G
18
GENIC
homozygous
45386565
20
5396546
5396547
T
C
21
GENIC
homozygous
45386569