chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
48700557
48700558
T
C
28
GENIC
homozygous
117002649
8
48700754
48700755
C
T
23
GENIC
homozygous
116957378
8
48700920
48700921
C
T
14
GENIC
homozygous
117002651
8
48700952
48700953
T
C
18
GENIC
homozygous
117002653
8
48700960
48700961
T
C
18
GENIC
homozygous
116957380
8
48701643
48701644
G
A
25
GENIC
homozygous
117002655
8
48701789
48701790
G
T
23
GENIC
homozygous
117002657
8
48702548
48702555
GTGATAG
37
GENIC
homozygous
132122136
8
48703057
48703057
TCTGAAGGGGCTGCTCCCAGAGAAGAAATGAAA
24
GENIC
possibly homozygous
132122137
8
48703303
48703304
C
T
15
GENIC
homozygous
117002659
8
48704121
48704122
T
C
26
GENIC
homozygous
117002661
8
48704601
48704602
G
A
15
GENIC
homozygous
117002663
8
48704613
48704614
C
T
14
GENIC
homozygous
117002665
8
48705490
48705491
C
T
13
GENIC
homozygous
117002667
8
48707324
48707325
C
T
15
GENIC
homozygous
117002669
8
48708004
48708005
A
G
18
GENIC
homozygous
117002671
8
48709424
48709425
A
G
25
GENIC
homozygous
117002673
8
48709706
48709707
A
G
21
GENIC
homozygous
117002675
8
48710518
48710519
T
C
27
GENIC
homozygous
117002677
8
48710964
48710965
G
A
26
GENIC
homozygous
117002679
8
48711179
48711180
T
A
16
GENIC
homozygous
117002681
8
48711323
48711324
A
G
22
GENIC
homozygous
117002683
