chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
20
6019752
6019753
G
A
41
GENIC
homozygous
109079787
20
6019789
6019790
A
C
51
GENIC
homozygous
109079791
20
6019871
6019872
C
T
58
GENIC
homozygous
109390649
20
6019937
6019938
A
G
55
GENIC
homozygous
109079793
20
6020335
6020336
G
A
39
GENIC
homozygous
109390650
20
6020953
6020954
A
G
49
GENIC
homozygous
109390651
20
6021130
6021131
G
A
61
GENIC
homozygous
109390652
20
6022121
6022122
G
C
34
GENIC
homozygous
109390653
20
6022692
6022693
A
G
34
GENIC
homozygous
109079795
20
6022752
6022753
T
G
39
GENIC
homozygous
109390654
20
6023206
6023207
C
T
54
GENIC
homozygous
109390655
20
6023258
6023259
T
C
50
GENIC
homozygous
109079799
20
6024964
6024965
C
T
41
GENIC
homozygous
109390656
20
6025120
6025121
T
A
36
GENIC
homozygous
109079803
20
6025440
6025441
G
T
43
GENIC
homozygous
109390657
20
6022020
6022020
TGTGTGTGCGAGTGCCTGTGTGCATGCCTGTGTGTGTGCGAGTGCCTGTGTGCATGCC
22
GENIC
homozygous
131555437
20
6022636
6022637
G
T
33
GENIC
homozygous
109234560
20
6022968
6022969
G
A
32
GENIC
homozygous
109595077
20
6025481
6025482
T
G
45
GENIC
homozygous
109547647
20
6025875
6025876
G
C
60
GENIC
homozygous
109079805
20
6025939
6025940
C
G
62
GENIC
possibly homozygous
109390658
20
6026788
6026789
T
A
51
GENIC
homozygous
109390659
20
6026800
6026801
T
C
50
GENIC
homozygous
109079807
20
6027101
6027101
G
7
GENIC
heterozygous
131555438
20
6027258
6027259
C
T
8
GENIC
possibly homozygous
119766824
