chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
49185069
49185070
C
T
5
GENIC
homozygous
52971489
8
49185172
49185173
G
A
13
GENIC
homozygous
52971490
8
49185218
49185219
C
T
9
GENIC
possibly homozygous
52971491
8
49185699
49185700
G
A
10
GENIC
homozygous
52971492
8
49186642
49186643
A
G
19
GENIC
possibly homozygous
52971493
8
49187126
49187127
C
T
11
GENIC
homozygous
52971494
8
49187188
49187189
T
C
8
GENIC
homozygous
52971495
8
49187268
49187269
A
G
12
GENIC
homozygous
52971496
8
49187461
49187462
C
CCAGTGGTCCTGCTGGGGGAATCAGTGATGGGATAAATGTGTGCATCCCTG
10
GENIC
homozygous
53363557
8
49187498
49187499
T
C
9
GENIC
homozygous
52971499
