chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
100782116
100782118
CA
--
4
GENIC
heterozygous
57578629
3
100783792
100783793
C
CTGGGTGTCTGGGTGTATGGTATGTGTGGTGTGTGTGTATGTGCGTGTGTGTGATGTGTGCATGTGTG
19
GENIC
homozygous
58617398
3
100788706
100788707
A
AC
23
GENIC
homozygous
57578641
3
100797333
100797334
T
TG
9
GENIC
homozygous
57578645
3
100797344
100797346
TG
--
10
GENIC
homozygous
57578647
3
100797349
100797351
AG
--
12
GENIC
homozygous
57578649
3
100799637
100799638
T
G
37
GENIC
homozygous
57578651
3
100799743
100799744
T
C
27
GENIC
homozygous
58555665
3
100799744
100799745
C
A
27
GENIC
homozygous
58555666
3
100799765
100799766
C
G
33
GENIC
homozygous
57578653
3
100799772
100799773
C
G
31
GENIC
homozygous
57578655
3
100799777
100799778
C
T
33
GENIC
homozygous
57578657
3
100799779
100799780
C
T
34
GENIC
homozygous
57578659
3
100799781
100799782
C
G
33
GENIC
homozygous
57578661
3
100799783
100799784
A
AC
32
GENIC
homozygous
57578663
3
100799791
100799792
C
A
32
GENIC
homozygous
57578667
3
100799799
100799800
T
G
32
GENIC
homozygous
57578669
3
100799809
100799810
C
G
30
GENIC
homozygous
57578671
3
100799815
100799816
T
A
33
GENIC
homozygous
57932699
3
100799816
100799817
C
G
33
GENIC
homozygous
57578673
3
100799818
100799819
C
G
33
GENIC
homozygous
57578675
3
100799832
100799833
C
T
31
GENIC
homozygous
57578677
3
100799841
100799842
C
A
29
GENIC
homozygous
57578679
