chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
161802581
161802582
C
T
60
GENIC
homozygous
141561676
3
161803824
161803825
A
G
52
GENIC
homozygous
141561677
3
161804118
161804119
C
T
59
GENIC
homozygous
143039411
3
161804293
161804294
T
G
52
GENIC
homozygous
141561678
3
161807037
161807038
G
A
49
GENIC
possibly homozygous
141561680
3
161807646
161807647
T
G
34
GENIC
homozygous
141561681
3
161810313
161810314
A
G
42
GENIC
homozygous
141561682
3
161810640
161810641
T
C
42
GENIC
homozygous
141561683
3
161810827
161810828
T
G
64
GENIC
homozygous
141561684
3
161813278
161813279
T
C
68
GENIC
homozygous
141561685
3
161810206
161810206
ACACACGT
41
GENIC
homozygous
141485989
3
161812054
161812081
GTGCCTTCCTGCACACTCTGCTCCAGC
34
GENIC
homozygous
143005143
3
161809345
161809360
GAGGGCCGTGATAAG
52
GENIC
possibly homozygous
141485987
3
161810058
161810061
GTG
42
GENIC
homozygous
141485988
