chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
49889353
49889354
G
GGTGTGTGTGTGTGTGTGT
4
GENIC
homozygous
50513821
12
49890647
49890648
A
ACC
2
GENIC
homozygous
50513823
12
49890689
49890690
A
AC
2
GENIC
homozygous
50235075
12
49891718
49891730
ACACACACACAC
------------
4
GENIC
heterozygous
50546756
12
49891720
49891730
ACACACACAC
----------
4
GENIC
heterozygous
50546757
12
49891952
49891953
T
C
33
GENIC
homozygous
50235079
12
49892515
49892516
A
G
24
GENIC
homozygous
50235081
12
49892564
49892565
C
CG
26
GENIC
homozygous
50235083
12
49892994
49892995
A
G
27
GENIC
homozygous
50235085
12
49893006
49893007
C
T
28
GENIC
homozygous
50235087
12
49895329
49895330
G
A
23
GENIC
homozygous
50623802
12
49895907
49895908
A
C
18
GENIC
homozygous
50235091
12
49896660
49896661
C
G
22
GENIC
homozygous
50623803
12
49896827
49896828
G
A
22
GENIC
homozygous
50623804
12
49897105
49897106
G
C
30
GENIC
homozygous
50235095
12
49897273
49897274
C
T
16
GENIC
homozygous
50623805
12
49897377
49897378
C
T
23
GENIC
homozygous
50623806
12
49898030
49898031
C
T
23
GENIC
homozygous
50623807
12
49899043
49899044
T
C
27
GENIC
homozygous
50235097
12
49899643
49899645
TG
--
25
GENIC
homozygous
50623808
12
49899940
49899941
A
AATAGGTAAGGGGTAGCTAGAAATGGGGACACTGAGACTGGTCAGGTCACACAGGTT
40
GENIC
homozygous
50546758
12
49900079
49900080
C
T
19
GENIC
homozygous
50623809
12
49900691
49900692
G
A
21
GENIC
homozygous
50235101
12
49902577
49902578
G
A
14
GENIC
homozygous
50235103
12
49902603
49902607
GGAG
----
7
GENIC
homozygous
50623810
12
49903130
49903131
C
A
37
GENIC
homozygous
50235105
12
49904879
49904883
AAAA
----
13
GENIC
possibly homozygous
50235119
12
49904882
49904883
A
ACC
11
GENIC
homozygous
50546761
12
49904882
49904883
A
-
13
GENIC
heterozygous
50471211
12
49907140
49907141
A
T
12
GENIC
homozygous
50235123
