chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
86202713
86202714
C
T
38
GENIC
homozygous
144416437
10
86203643
86203643
C
33
GENIC
homozygous
138696983
10
86203718
86203751
CTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTT
16
GENIC
possibly homozygous
144412379
10
86204239
86204245
GAGGGA
34
GENIC
homozygous
144412380
10
86204985
86204986
T
C
39
GENIC
homozygous
144416438
10
86205194
86205195
C
51
GENIC
homozygous
138696984
10
86205683
86205684
A
G
55
GENIC
homozygous
144416439
10
86206246
86206247
C
45
GENIC
homozygous
403293736
10
86206246
86206247
C
A
45
GENIC
heterozygous
403293737
10
86203750
86203751
T
16
GENIC
possibly homozygous
403293734
10
86203750
86203751
T
C
16
GENIC
heterozygous
403293735
10
86207529
86207530
C
G
56
GENIC
homozygous
144416440
10
86208239
86208240
C
T
47
GENIC
homozygous
144416441
10
86209969
86209969
TG
32
GENIC
homozygous
144412381
10
86210040
86210041
C
23
GENIC
homozygous
138696986
10
86210400
86210401
T
C
51
GENIC
homozygous
144416442
10
86210953
86210954
C
T
61
GENIC
homozygous
144416443
10
86215373
86215374
C
T
50
GENIC
homozygous
144416444
10
86216035
86216036
T
A
41
GENIC
homozygous
144416445
10
86216574
86216575
C
A
13
GENIC
homozygous
144416446
10
86216636
86216637
C
7
GENIC
homozygous
144412382
10
86217136
86217137
T
C
30
GENIC
homozygous
144416447
10
86218272
86218273
A
G
52
GENIC
homozygous
144416448
