chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
14273580
14273581
C
T
47
GENIC
homozygous
111452642
3
14273624
14273625
A
G
42
GENIC
homozygous
111452643
3
14274704
14274705
G
A
62
GENIC
homozygous
111452644
3
14275484
14275485
T
C
37
GENIC
homozygous
111452645
3
14276278
14276279
A
T
59
GENIC
homozygous
111452646
3
14276371
14276372
T
C
37
GENIC
homozygous
111452647
3
14277114
14277115
G
A
32
GENIC
possibly homozygous
111452648
3
14277551
14277552
T
C
38
GENIC
homozygous
111452649
3
14278498
14278498
AGAC
13
GENIC
homozygous
127851834
3
14276174
14276175
A
43
GENIC
homozygous
127851832
3
14278547
14278548
T
C
30
GENIC
homozygous
111452651
3
14279077
14279078
G
A
37
GENIC
homozygous
111452652
3
14280167
14280168
G
A
42
GENIC
homozygous
111452653
3
14281275
14281275
TGGGGATTTAGCTCAGTGGTAGAGCG
20
GENIC
homozygous
127851835
3
14281280
14281280
CTAGCAAGCA
29
GENIC
homozygous
127851836
3
14281869
14281870
C
T
38
GENIC
homozygous
111452654
3
14285943
14285944
G
A
38
GENIC
homozygous
111452655
3
14286937
14286937
TA
48
GENIC
homozygous
127851837
3
14287598
14287599
T
A
37
GENIC
homozygous
111452657
3
14281278
14281279
T
G
29
GENIC
homozygous
127968578
3
14286280
14286281
T
C
52
GENIC
homozygous
111452656
3
14287666
14287667
G
33
GENIC
homozygous
127851838