chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
5
129511891
129511892
C
T
61
GENIC
possibly homozygous
143959125
5
129512603
129512604
C
T
46
GENIC
homozygous
143959126
5
129512840
129512841
A
T
58
GENIC
homozygous
143959127
5
129515800
129515801
C
G
54
GENIC
homozygous
143959128
5
129516963
129516964
A
C
45
GENIC
homozygous
143959129
5
129518141
129518257
CTACAGACTGTATTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCTTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC
42
GENIC
homozygous
143943613
5
129518794
129518798
ATAT
46
GENIC
homozygous
143943614
5
129519412
129519413
A
G
53
GENIC
homozygous
143959130
5
129519983
129519984
G
A
64
GENIC
homozygous
143959131
5
129520124
129520125
C
T
69
GENIC
homozygous
143959132
5
129520490
129520491
C
T
56
GENIC
homozygous
137620186
5
129522946
129522946
GA
60
GENIC
possibly homozygous
143943615
5
129523786
129523787
G
A
62
GENIC
homozygous
143959133
5
129523992
129523993
C
T
53
GENIC
homozygous
143959134
5
129525414
129525415
T
C
63
GENIC
homozygous
143959135
5
129526118
129526118
CTTTTCTTTTC
14
GENIC
heterozygous
146771172
5
129526168
129526169
C
T
35
GENIC
homozygous
146140766
5
129526277
129526278
G
C
67
GENIC
homozygous
143959136
5
129527969
129527970
C
T
64
GENIC
homozygous
143959137
5
129528331
129528335
TAAA
56
GENIC
homozygous
143943616
5
129528501
129528502
T
G
47
GENIC
homozygous
137620190
5
129528533
129528534
C
T
48
GENIC
homozygous
143959138
5
129528917
129528920
CAG
40
GENIC
homozygous
143943617
5
129531345
129531346
G
A
50
GENIC
homozygous
143959139
5
129532275
129532276
G
A
51
GENIC
homozygous
143959140
5
129526037
129526038
G
C
19
GENIC
heterozygous
403600041
5
129526037
129526038
G
19
GENIC
heterozygous
403600040
