chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
51548782
51548783
A
C
15
GENIC
homozygous
116594416
10
51554657
51554657
G
8
GENIC
homozygous
128817098
10
51561007
51561008
T
C
3
GENIC
homozygous
123358740
10
51561007
51561007
C
3
GENIC
homozygous
128817103
10
51561010
51561015
TGTTA
3
GENIC
homozygous
128817104
10
51561017
51561017
TAGG
2
GENIC
homozygous
128817105
10
51561020
51561022
AA
2
GENIC
homozygous
128817106
10
51561026
51561027
G
C
3
GENIC
homozygous
123358745
10
51561028
51561029
T
C
3
GENIC
homozygous
123358746
10
51586004
51586005
C
A
14
GENIC
homozygous
117994137
10
51594207
51594207
C
8
GENIC
homozygous
128817118
10
51594212
51594213
G
8
GENIC
homozygous
128817119
10
51594260
51594262
GC
13
GENIC
homozygous
128817120
10
51594295
51594295
A
18
GENIC
homozygous
128817121
10
51594299
51594299
G
20
GENIC
homozygous
128817122
10
51594372
51594372
T
20
GENIC
homozygous
128817123
10
51594379
51594379
T
20
GENIC
homozygous
128817124
10
51594446
51594446
T
10
GENIC
homozygous
128817125
10
51594468
51594469
G
A
10
GENIC
homozygous
116594522
10
51594480
51594480
A
10
GENIC
homozygous
128817126
10
51594507
51594507
T
8
GENIC
homozygous
128817127
10
51594517
51594517
C
7
GENIC
homozygous
128817128
10
51561070
51561071
G
A
3
GENIC
homozygous
117078291
10
51574954
51574955
G
12
GENIC
heterozygous
131093536
10
51588922
51588922
T
18
GENIC
heterozygous
130681810
10
51656353
51656353
C
23
GENIC
homozygous
128817148
10
51657396
51657396
C
15
GENIC
homozygous
128817149
10
51657400
51657400
AC
15
GENIC
homozygous
128817150
10
51657408
51657409
C
12
GENIC
homozygous
128817151
10
51657530
51657530
TGT
17
GENIC
homozygous
128817152
10
51657610
51657635
TTCTTCTCCTCTTCTCTCATCTCTC
1
GENIC
homozygous
130576713
10
51657684
51657684
C
1
GENIC
homozygous
129969015
10
51657527
51657528
C
G
17
GENIC
homozygous
116884939
