chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
50140469
50140470
G
A
68
GENIC
homozygous
116815382
8
50140919
50140920
A
T
51
GENIC
homozygous
116815384
8
50141637
50141638
A
G
61
GENIC
homozygous
116815386
8
50144282
50144283
C
T
53
GENIC
homozygous
116815388
8
50145904
50145905
A
G
30
GENIC
homozygous
116815392
8
50147252
50147253
C
T
45
GENIC
homozygous
116815394
8
50147870
50147871
A
G
48
GENIC
homozygous
116815396
8
50151350
50151351
G
A
53
GENIC
homozygous
116815398
8
50151558
50151559
C
T
49
GENIC
homozygous
116815400
8
50151949
50151950
C
A
48
GENIC
homozygous
116815402
8
50151955
50151956
C
G
48
GENIC
homozygous
116815404
8
50153611
50153612
G
A
34
GENIC
homozygous
116815414
8
50153978
50153979
G
A
26
GENIC
homozygous
116815416
8
50154824
50154825
A
G
58
GENIC
homozygous
116815418
8
50156314
50156315
A
G
62
GENIC
homozygous
116815420
8
50158325
50158326
T
C
54
GENIC
homozygous
116815422
8
50159066
50159067
G
A
43
GENIC
homozygous
116815424
8
50159196
50159197
G
C
35
GENIC
homozygous
116815426
8
50159318
50159319
C
T
38
GENIC
homozygous
116815428
8
50160037
50160038
C
T
45
GENIC
homozygous
116815430
8
50153881
50153882
G
22
GENIC
homozygous
130361722
8
50145831
50145832
T
25
GENIC
homozygous
130361719
8
50145835
50145835
CCT
23
GENIC
possibly homozygous
130361720
8
50153184
50153264
TGGGGTACACTCTAGGATGAAATGTTAGAACTCTGGCTCCTGGGGTACACTCTAGGAGGAGATATTAGAACTGTGGCTCT
29
GENIC
homozygous
130361721
8
50145832
50145833
T
G
25
GENIC
homozygous
117927958
