chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
10775101
10775102
G
A
19
GENIC
homozygous
116493695
10
10775351
10775352
T
C
15
GENIC
homozygous
116493697
10
10775701
10775701
TTTTG
10
GENIC
homozygous
131087101
10
10776154
10776155
A
G
15
GENIC
homozygous
116493699
10
10776268
10776269
C
T
15
GENIC
homozygous
116493701
10
10776837
10776838
C
T
20
GENIC
homozygous
116493703
10
10777390
10777391
C
T
19
GENIC
homozygous
116493705
10
10777433
10777434
G
A
14
GENIC
homozygous
116493707
10
10778194
10778195
T
G
9
GENIC
homozygous
116493709
10
10778196
10778197
G
T
10
GENIC
homozygous
116493711
10
10778404
10778484
ACACACATACACACACATATACACACACATACATACACACATAAGCACATACATACACACACATACACACACACATACAC
5
GENIC
heterozygous
131087102
10
10778558
10778558
AC
13
GENIC
homozygous
131087103
10
10778650
10778652
AC
7
GENIC
homozygous
131087104
10
10778639
10778640
T
C
8
GENIC
homozygous
118026515
10
10778579
10778580
T
C
10
GENIC
homozygous
117981154
10
10778631
10778632
C
T
9
GENIC
homozygous
131099869
10
10778633
10778634
T
C
9
GENIC
homozygous
131099870
10
10779448
10779449
A
G
20
GENIC
homozygous
116493713
10
10779804
10779805
G
A
14
GENIC
homozygous
116493715
10
10780292
10780294
CT
9
GENIC
homozygous
128789529
10
10780307
10780309
AT
9
GENIC
homozygous
128789530
10
10780382
10780383
G
A
21
GENIC
homozygous
116493717
10
10780412
10780413
T
A
22
GENIC
homozygous
116493719
10
10780413
10780414
C
A
22
GENIC
homozygous
116493721
10
10782736
10782737
T
C
24
GENIC
homozygous
116493723
10
10782804
10782805
G
A
23
GENIC
homozygous
116493725
10
10784266
10784267
G
A
14
GENIC
homozygous
116734081
10
10779706
10779707
C
T
12
GENIC
homozygous
117102508
10
10779719
10779720
C
T
13
GENIC
homozygous
117140125
10
10780296
10780297
C
T
9
GENIC
homozygous
117119890
10
10783067
10783068
G
T
22
GENIC
homozygous
116734080
