chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
15
44791093
44791094
C
T
31
GENIC
homozygous
147806690
15
44791276
44791277
C
T
26
GENIC
homozygous
139726731
15
44791737
44791738
A
G
19
GENIC
homozygous
147806691
15
44792258
44792259
A
G
20
GENIC
homozygous
139726732
15
44792756
44792757
G
C
19
GENIC
homozygous
147806692
15
44793388
44793389
G
A
24
GENIC
homozygous
147806693
15
44795148
44795148
TA
24
GENIC
homozygous
147803054
15
44795520
44795521
C
T
28
GENIC
homozygous
147806694
15
44795960
44795961
C
T
26
GENIC
homozygous
139726737
15
44797097
44797098
C
T
23
GENIC
homozygous
147806695
15
44798711
44798712
T
C
20
GENIC
homozygous
147806696
15
44798713
44798714
A
T
22
GENIC
homozygous
147806697
15
44798780
44798782
AT
12
GENIC
homozygous
139632085
15
44799151
44799151
CAAAGATGCATATGCACAGATCTAG
21
GENIC
homozygous
139632086
15
44799209
44799210
G
T
23
GENIC
homozygous
147806698
15
44799267
44799268
G
C
15
GENIC
homozygous
139726738
15
44799477
44799478
G
A
20
GENIC
homozygous
139726740
15
44800392
44800393
C
G
9
GENIC
homozygous
139726749
15
44801017
44801018
G
A
17
GENIC
homozygous
147806699
15
44801068
44801069
A
G
22
GENIC
homozygous
147806700
15
44803206
44803207
G
A
22
GENIC
homozygous
147806701
15
44803707
44803708
G
A
24
GENIC
homozygous
147806702
15
44804490
44804491
G
A
25
GENIC
homozygous
147806703
15
44805200
44805201
A
G
29
GENIC
homozygous
147806704
15
44805312
44805315
TTC
18
GENIC
homozygous
139632088
15
44805316
44805317
G
18
GENIC
homozygous
139632089
15
44805318
44805319
G
A
19
GENIC
homozygous
139726754
15
44805654
44805655
C
T
34
GENIC
homozygous
147806705
15
44800374
44800375
C
8
GENIC
possibly homozygous
403855538
15
44798781
44798782
T
C
12
GENIC
heterozygous
154890494
15
44798781
44798782
T
12
GENIC
homozygous
403855536
15
44800374
44800375
C
G
8
GENIC
heterozygous
403855537
