chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
15
51385483
51385484
C
T
15
GENIC
homozygous
112682369
15
51385666
51385667
C
T
19
GENIC
homozygous
112507172
15
51386648
51386649
A
G
18
GENIC
possibly homozygous
112507174
15
51387146
51387147
G
C
18
GENIC
possibly homozygous
112682371
15
51387778
51387779
G
A
17
GENIC
homozygous
112682373
15
51389910
51389911
C
T
27
GENIC
homozygous
112682375
15
51390350
51390351
C
T
21
GENIC
homozygous
112507185
15
51391487
51391488
C
T
23
GENIC
homozygous
112682377
15
51393101
51393102
T
C
16
GENIC
homozygous
112682379
15
51393103
51393104
A
T
16
GENIC
homozygous
112682381
15
51393541
51393541
CAAAGATGCATATGCACAGATCTAG
22
GENIC
homozygous
129255656
15
51386127
51386128
A
G
17
GENIC
homozygous
112988367
15
51389538
51389538
TA
13
GENIC
homozygous
134027346
15
51393170
51393172
AT
20
GENIC
homozygous
129255655
15
51393599
51393600
G
T
19
GENIC
homozygous
112682383
15
51393657
51393658
G
C
15
GENIC
homozygous
112507187
15
51393867
51393868
G
A
16
GENIC
homozygous
112507191
15
51394782
51394783
C
G
11
GENIC
homozygous
124076419
15
51395407
51395408
G
A
19
GENIC
homozygous
112682385
15
51395458
51395459
A
G
15
GENIC
homozygous
112682387
15
51397596
51397597
G
A
13
GENIC
homozygous
112682389
15
51398097
51398098
G
A
26
GENIC
homozygous
113171091
15
51398141
51398142
A
22
GENIC
heterozygous
130592670
15
51398880
51398881
G
A
24
GENIC
homozygous
112682390
15
51399590
51399591
A
G
17
GENIC
homozygous
112682392
15
51399702
51399705
TTC
12
GENIC
homozygous
129255658
15
51399706
51399707
G
12
GENIC
homozygous
129255659
15
51399708
51399709
G
A
12
GENIC
homozygous
112507205
15
51400044
51400045
C
T
21
GENIC
homozygous
112682394
