chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
90502205
90502206
G
C
32
GENIC
homozygous
61462328
1
90503113
90503114
C
-
10
GENIC
homozygous
62569689
1
90503115
90503140
CTCTCTCTCTCTCTCTCTCTCTCTC
-------------------------
12
GENIC
homozygous
62534948
1
90503588
90503589
G
A
25
GENIC
homozygous
61888169
1
90504259
90504260
C
T
11
GENIC
homozygous
61888170
1
90504528
90504529
T
C
22
GENIC
homozygous
61462332
1
90504968
90504969
C
CTTTT
7
GENIC
heterozygous
62140640
1
90504969
90504970
T
-
7
GENIC
heterozygous
62311333
1
90505045
90505046
A
G
21
GENIC
possibly homozygous
61462334
1
90505106
90505107
A
G
16
GENIC
homozygous
61462335
1
90507347
90507348
T
C
28
GENIC
homozygous
61462341
1
90507868
90507869
C
T
23
GENIC
homozygous
61462343
1
90508250
90508251
T
C
16
GENIC
homozygous
61462345
1
90509102
90509103
T
TAAA
21
GENIC
homozygous
61888171
1
90509821
90509822
G
GTGAATGAATGAATGAATGAATGAA
8
GENIC
homozygous
62650118
1
90511931
90511932
C
-
15
GENIC
homozygous
61462350
1
90512343
90512344
A
G
24
GENIC
heterozygous
62264060
1
90513060
90513061
T
C
42
GENIC
homozygous
61462357
1
90513845
90513846
A
G
30
GENIC
homozygous
61462361
1
90514473
90514474
C
A
32
GENIC
homozygous
61462363
1
90516248
90516249
G
A
34
GENIC
homozygous
61462365
