chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
172195462
172195463
C
T
3
GENIC
homozygous
112258444
3
172201938
172201939
C
G
14
GENIC
homozygous
112208947
3
172196989
172196989
CTT
13
GENIC
homozygous
130915666
3
172197657
172197658
T
C
14
GENIC
homozygous
112208938
3
172200431
172200432
A
T
16
GENIC
homozygous
112208939
3
172200450
172200451
G
A
13
GENIC
homozygous
112208941
3
172200612
172200613
C
G
16
GENIC
homozygous
112208943
3
172201848
172201849
A
C
19
GENIC
homozygous
112208945
3
172202006
172202007
A
G
7
GENIC
homozygous
112208949
3
172202007
172202008
T
C
6
GENIC
homozygous
112208951
3
172202980
172202981
T
C
15
GENIC
homozygous
112208953
3
172204584
172204620
CACACGCGCACACACACACACACGCGCACACGCGCG
14
GENIC
homozygous
130915667
3
172204763
172204763
GTGCCCACACGCGCACACGCACAC
22
GENIC
homozygous
130915668
3
172204815
172204816
A
G
16
GENIC
homozygous
112208957
3
172205947
172205948
A
G
16
GENIC
homozygous
112208959
3
172206514
172206515
A
G
11
GENIC
homozygous
112208961
3
172206690
172206691
T
C
16
GENIC
homozygous
112208963
3
172207118
172207119
T
C
14
GENIC
homozygous
112208965