chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
95770683
95770684
T
G
31
GENIC
heterozygous
116688144
10
95770683
95770683
G
31
GENIC
heterozygous
130682379
10
95803078
95803078
G
16
GENIC
homozygous
128848817
10
95803082
95803082
G
16
GENIC
homozygous
128848818
10
95803097
95803097
G
13
GENIC
possibly homozygous
128848819
10
95803102
95803102
G
13
GENIC
possibly homozygous
128848820
10
95803107
95803107
G
11
GENIC
possibly homozygous
128848821
10
95803155
95803156
T
13
GENIC
homozygous
128848823
10
95803159
95803159
T
14
GENIC
homozygous
128848824
10
95830142
95830142
A
23
GENIC
homozygous
129970562
10
95830146
95830148
TG
24
GENIC
homozygous
129970563
10
95830204
95830206
TG
27
GENIC
heterozygous
133232975
10
95850924
95850924
C
41
GENIC
homozygous
128848836
10
95850944
95850944
A
36
GENIC
homozygous
128848837
10
95850991
95850991
T
33
GENIC
homozygous
128848838
10
95850995
95850995
C
32
GENIC
homozygous
128848839
10
95851074
95851075
T
14
GENIC
homozygous
129970564
10
95852082
95852083
T
51
GENIC
homozygous
128848841
10
95865298
95865299
T
C
16
GENIC
possibly homozygous
118009693
10
95893814
95893814
G
53
GENIC
homozygous
128848853
10
95898290
95898290
AAATGTGTGCTTAGCAGGAAAGTGTAGGGAGCAAGGAATGACTCCAGCTCTCAGAGCCGGATGCTGCGGGGAGCACATATTTTTGGGAC
35
GENIC
homozygous
128848854
10
95850976
95850977
C
T
35
GENIC
homozygous
117328786
10
95850978
95850979
T
A
34
GENIC
homozygous
117328788
10
95853062
95853062
A
20
GENIC
heterozygous
133968640