chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
9
94302276
94302277
G
T
13
GENIC
homozygous
117605035
9
94302590
94302591
G
A
15
GENIC
homozygous
117605037
9
94302760
94302760
G
12
GENIC
homozygous
128733214
9
94303107
94303108
C
T
16
GENIC
homozygous
117605039
9
94303388
94303507
AACAAAAAGAGAGCAGGGGGGCTGGGGATTTAGCTCAGTGGTAGAACGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAGAACCAAAAAAAAAACAAA
15
GENIC
possibly homozygous
128733215
9
94306125
94306126
A
G
24
GENIC
homozygous
117605043
9
94306138
94306139
C
A
30
GENIC
homozygous
117605045
9
94306140
94306141
T
C
30
GENIC
homozygous
117605047
9
94307058
94307059
A
G
22
GENIC
homozygous
117605049
9
94303358
94303359
G
A
16
GENIC
homozygous
117601999
9
94306113
94306114
A
21
GENIC
homozygous
128733216
9
94306123
94306124
A
24
GENIC
homozygous
128733217
9
94303703
94303704
G
A
31
GENIC
homozygous
117602001
9
94306008
94306009
G
C
18
GENIC
homozygous
117602003
9
94304517
94304517
A
28
GENIC
homozygous
132135240
9
94307796
94307797
G
A
16
GENIC
homozygous
117602005