chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
5
122917335
122917335
CCT
49
GENIC
homozygous
137338148
5
122918157
122918158
T
C
44
GENIC
homozygous
137608338
5
122918551
122918552
C
G
46
GENIC
homozygous
137608339
5
122918895
122918896
T
C
20
GENIC
homozygous
137608340
5
122919311
122919312
T
G
48
GENIC
homozygous
137608341
5
122920304
122920304
AAAAGTGATTAATAGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAA
20
GENIC
homozygous
146771058
5
122920590
122920590
G
12
GENIC
homozygous
141688681
5
122920667
122920668
C
T
22
GENIC
homozygous
141756531
5
122920859
122920860
C
T
51
GENIC
homozygous
137608346
5
122927723
122927724
C
T
44
GENIC
heterozygous
141756538
5
122929979
122929980
T
A
39
GENIC
homozygous
137608352
5
122930384
122930385
C
T
48
GENIC
possibly homozygous
143953377
5
122920268
122920269
C
T
35
GENIC
homozygous
143953374
5
122923299
122923300
T
C
48
GENIC
homozygous
143953375
5
122929949
122929950
A
T
39
GENIC
possibly homozygous
143953376
5
122921070
122921070
A
44
GENIC
homozygous
143942571
5
122931222
122931223
G
A
38
GENIC
homozygous
143953378
5
122931427
122931428
C
A
49
GENIC
homozygous
143953379
5
122931538
122931538
GGTATGTT
44
GENIC
homozygous
137338153
5
122931773
122931774
C
T
45
GENIC
homozygous
143953380
5
122932032
122932032
CT
38
GENIC
homozygous
137338154
5
122932252
122932253
A
G
49
GENIC
homozygous
137608357
5
122932307
122932308
G
A
45
GENIC
homozygous
143953381
5
122932817
122932818
G
T
53
GENIC
homozygous
143953382
5
122933215
122933216
T
C
41
GENIC
homozygous
143953383
5
122933287
122933288
T
C
39
GENIC
homozygous
137608360
5
122933964
122933965
C
A
44
GENIC
homozygous
137608362
5
122933728
122933729
G
C
50
GENIC
homozygous
154329326
5
122924798
122924799
A
G
8
GENIC
homozygous
403156129
5
122933728
122933729
G
A
50
GENIC
heterozygous
154329325
