chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
4
157646292
157646293
T
C
13
GENIC
homozygous
137248762
4
157646546
157646547
A
T
14
GENIC
homozygous
137248763
4
157646792
157646793
G
T
16
GENIC
homozygous
137248764
4
157646855
157646856
G
A
12
GENIC
homozygous
137248765
4
157647329
157647330
A
G
15
GENIC
homozygous
137248766
4
157647658
157647659
G
C
16
GENIC
homozygous
137248767
4
157648999
157649000
C
T
16
GENIC
homozygous
137248768
4
157649488
157649489
T
C
15
GENIC
homozygous
137248769
4
157649932
157649933
G
A
16
GENIC
homozygous
137248770
4
157649978
157649979
A
T
14
GENIC
homozygous
137248771
4
157650336
157650337
A
G
15
GENIC
homozygous
137248772
4
157651004
157651005
G
C
12
GENIC
homozygous
137248773
4
157652973
157652974
G
A
11
GENIC
homozygous
137248774
4
157653090
157653091
C
T
19
GENIC
homozygous
137248775
4
157653319
157653320
T
C
20
GENIC
homozygous
137248776
4
157648901
157648901
GTTTTGTTTTGTTTTG
13
GENIC
homozygous
136925256
4
157649696
157649696
G
16
GENIC
homozygous
136925257
4
157653173
157653176
TCC
22
GENIC
homozygous
136925258
4
157654967
157654968
G
A
12
GENIC
homozygous
137248777
4
157657489
157657489
TGA
15
GENIC
homozygous
136925259
4
157657572
157657674
GCGCTTGCTAGGCAAGGGCTCTACCACTGAGCTAAATCCCCAACCCCGTTGATGTTGTTTTAAGGCAAGATCTCGGGGTTGGGGATTTAGCTCAGTGGTAGA
11
GENIC
heterozygous
136925260
4
157658238
157658239
C
T
4
GENIC
homozygous
137248778
4
157658549
157658550
C
A
13
GENIC
homozygous
137248779
4
157659133
157659134
G
A
14
GENIC
homozygous
137248780
4
157659834
157659835
A
G
20
GENIC
homozygous
137248781
4
157660727
157660735
TCTCTGTC
11
GENIC
homozygous
136925261
4
157661632
157661633
A
G
11
GENIC
homozygous
137248782
4
157661730
157661731
C
G
11
GENIC
homozygous
137248783
4
157654956
157654957
G
A
10
GENIC
homozygous
403125163
4
157657502
157657503
T
G
12
GENIC
heterozygous
154221634
4
157654956
157654957
G
10
GENIC
heterozygous
403125164
4
157657502
157657503
T
12
GENIC
homozygous
403125165
4
157655173
157655175
GG
8
GENIC
heterozygous
146091951
