chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
13
52124844
52124845
G
55
GENIC
homozygous
133261257
13
52125147
52125148
C
T
34
GENIC
homozygous
114764126
13
52125738
52125739
G
A
47
GENIC
homozygous
114764128
13
52125861
52125862
A
G
42
GENIC
homozygous
114764130
13
52126335
52126336
T
C
57
GENIC
homozygous
114764132
13
52126644
52126645
C
T
54
GENIC
homozygous
114764134
13
52127088
52127089
T
G
47
GENIC
homozygous
114764136
13
52127231
52127232
T
G
45
GENIC
homozygous
114764138
13
52127441
52127442
A
G
41
GENIC
possibly homozygous
114764140
13
52128026
52128026
A
39
GENIC
homozygous
133261258
13
52128347
52128348
G
C
43
GENIC
homozygous
114764142
13
52128493
52128494
A
G
49
GENIC
homozygous
114764144
13
52125186
52125186
CTTAAAAGTTTGTGCTACACTATAGCTGTAGTCTCAGTTTCTT
28
GENIC
homozygous
129053766
13
52127603
52127604
T
C
27
GENIC
homozygous
114672475
13
52128849
52128850
C
T
33
GENIC
homozygous
114764146
13
52129248
52129249
G
T
42
GENIC
homozygous
114764148
13
52129508
52129509
T
C
49
GENIC
homozygous
114764150
13
52129898
52129899
G
A
39
GENIC
homozygous
114764152
13
52130862
52130863
C
T
34
GENIC
homozygous
114764154
13
52131792
52131793
T
C
52
GENIC
homozygous
114345479
13
52131981
52131982
G
A
47
GENIC
homozygous
114345481
13
52132378
52132379
A
40
GENIC
possibly homozygous
129053769
13
52132650
52132651
A
C
48
GENIC
homozygous
114345483
13
52132994
52132995
C
T
35
GENIC
homozygous
114345485
13
52134808
52134808
TTA
50
GENIC
homozygous
129053771
13
52135947
52135948
T
C
40
GENIC
homozygous
114345489
13
52136067
52136068
G
A
54
GENIC
homozygous
114764156
13
52132740
52132741
A
G
58
GENIC
homozygous
114857687
13
52129043
52129044
A
G
33
GENIC
homozygous
115182449
13
52130259
52130260
G
A
31
GENIC
homozygous
115182451
13
52131567
52131568
G
T
48
GENIC
homozygous
115152185