chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
62076662
62076663
T
-
20
GENIC
homozygous
54149950
8
62076663
62076664
T
A
21
GENIC
homozygous
54149952
8
62076799
62076800
A
G
17
GENIC
homozygous
54149954
8
62076925
62076927
TT
--
21
GENIC
heterozygous
53320102
8
62076926
62076927
T
-
21
GENIC
heterozygous
53433697
8
62077928
62077929
C
CT
19
GENIC
possibly homozygous
52989885
8
62078777
62078778
A
G
30
GENIC
possibly homozygous
52989891
8
62079268
62079280
ATTCATTCATTC
------------
21
GENIC
homozygous
54149956
8
62081252
62081253
G
T
20
GENIC
possibly homozygous
54149958
8
62082033
62082034
T
-
11
GENIC
heterozygous
52989906
8
62086359
62086391
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
--------------------------------
27
GENIC
possibly homozygous
53902768
8
62086412
62086413
T
C
10
GENIC
possibly homozygous
54149960
8
62086414
62086415
T
C
10
GENIC
possibly homozygous
54149962
8
62086416
62086417
T
C
9
GENIC
possibly homozygous
53389337
8
62086418
62086419
T
C
9
GENIC
possibly homozygous
53208197
8
62086420
62086421
T
C
16
GENIC
possibly homozygous
52989918
8
62086808
62086809
A
G
25
GENIC
possibly homozygous
52989920
8
62086950
62086951
C
A
26
GENIC
possibly homozygous
52989922