chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
95770683
95770684
T
G
14
GENIC
homozygous
116688144
10
95803078
95803078
G
10
GENIC
homozygous
128848817
10
95803082
95803082
G
10
GENIC
homozygous
128848818
10
95803097
95803097
G
10
GENIC
homozygous
128848819
10
95803102
95803102
G
10
GENIC
homozygous
128848820
10
95803107
95803107
G
10
GENIC
homozygous
128848821
10
95803155
95803156
T
6
GENIC
homozygous
128848823
10
95803159
95803159
T
6
GENIC
homozygous
128848824
10
95850924
95850924
C
13
GENIC
homozygous
128848836
10
95850944
95850944
A
10
GENIC
homozygous
128848837
10
95850991
95850991
T
11
GENIC
homozygous
128848838
10
95850995
95850995
C
12
GENIC
homozygous
128848839
10
95852082
95852083
T
27
GENIC
homozygous
128848841
10
95853002
95853003
A
G
5
GENIC
heterozygous
118009690
10
95865298
95865299
T
C
7
GENIC
possibly homozygous
118009693
10
95886599
95886600
T
23
GENIC
heterozygous
128848852
10
95893814
95893814
G
17
GENIC
homozygous
128848853
10
95898290
95898290
AAATGTGTGCTTAGCAGGAAAGTGTAGGGAGCAAGGAATGACTCCAGCTCTCAGAGCCGGATGCTGCGGGGAGCACATATTTTTGGGAC
13
GENIC
homozygous
128848854
10
95830142
95830142
A
10
GENIC
homozygous
129970562
10
95830146
95830148
TG
8
GENIC
homozygous
129970563
10
95851074
95851075
T
8
GENIC
homozygous
129970564
10
95821161
95821162
G
T
14
GENIC
heterozygous
134064958
10
95850976
95850977
C
T
13
GENIC
homozygous
117328786
10
95850978
95850979
T
A
13
GENIC
homozygous
117328788