chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
14
17027792
17027793
A
G
36
GENIC
homozygous
139462031
14
17027800
17027801
C
T
41
GENIC
homozygous
139462032
14
17028610
17028611
T
C
35
GENIC
homozygous
139462033
14
17028983
17028984
G
A
28
GENIC
homozygous
403353401
14
17028979
17028980
G
A
28
GENIC
homozygous
403353399
14
17028979
17028980
G
28
GENIC
heterozygous
403353400
14
17028983
17028984
G
28
GENIC
heterozygous
403353402
14
17030254
17030255
C
12
GENIC
heterozygous
403353403
14
17032010
17032011
A
G
34
GENIC
homozygous
139462034
14
17032984
17032985
G
A
52
GENIC
homozygous
139462035
14
17033139
17033140
A
G
22
GENIC
possibly homozygous
139462036
14
17033143
17033144
A
G
22
GENIC
possibly homozygous
139462037
14
17030254
17030255
C
G
12
GENIC
possibly homozygous
154827179
14
17033135
17033135
AG
22
GENIC
possibly homozygous
139381805
14
17033148
17033148
GGGAGGGAGGGAGGAAGG
21
GENIC
homozygous
139381807
14
17033146
17033146
GG
22
GENIC
possibly homozygous
139381806
14
17029016
17029042
TATATGTGTGTGTGTGTGTGTATTTA
35
GENIC
homozygous
139381804
14
17033642
17033643
T
C
55
GENIC
homozygous
139462038
14
17034716
17034717
T
C
51
GENIC
homozygous
139462039
14
17034991
17034991
CT
58
GENIC
homozygous
139381808
14
17036013
17036014
G
A
42
GENIC
homozygous
139462040
14
17038139
17038140
T
C
38
GENIC
homozygous
139462041
14
17038900
17038901
T
C
38
GENIC
homozygous
139462042
14
17039147
17039148
A
G
46
GENIC
homozygous
139462043
14
17039765
17039766
T
C
49
GENIC
homozygous
139462044
14
17040627
17040628
A
35
GENIC
homozygous
139381809
14
17035511
17035511
CTGTAGTCATGGTGATGGCTGTAGTCATGGTGATGG
1
GENIC
homozygous
145825630
