chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
13
50530360
50530361
G
A
52
GENIC
homozygous
114890182
13
50530503
50530504
G
A
49
GENIC
homozygous
114340704
13
50531089
50531090
G
C
44
GENIC
homozygous
114340706
13
50531351
50531355
GTTT
38
GENIC
homozygous
129052769
13
50531632
50531633
C
T
67
GENIC
homozygous
114890184
13
50531949
50531950
C
T
67
GENIC
homozygous
114340710
13
50533753
50533754
T
C
34
GENIC
homozygous
114340715
13
50534211
50534212
C
T
35
GENIC
homozygous
114890186
13
50534382
50534389
ACCCCAG
43
GENIC
homozygous
131126386
13
50536215
50536216
C
A
46
GENIC
possibly homozygous
114890188
13
50536435
50536436
G
A
38
GENIC
homozygous
114890190
13
50535475
50535501
CACTCTTTCTCACACAAACACTCACG
31
GENIC
heterozygous
131501775
