chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
45060252
45060253
A
G
11
GENIC
homozygous
51635936
10
45060287
45060288
A
C
24
GENIC
homozygous
51635937
10
45060662
45060663
T
A
10
GENIC
heterozygous
51441655
10
45060835
45060836
T
TTTGGTTGGTTGG
11
GENIC
possibly homozygous
51635940
10
45060843
45060844
G
T
11
GENIC
possibly homozygous
51635942
10
45060879
45060880
G
-
7
GENIC
homozygous
51441656
10
45061285
45061286
C
T
13
GENIC
possibly homozygous
51635943
10
45061841
45061842
T
C
19
GENIC
possibly homozygous
51635944
10
45062416
45062417
T
G
24
GENIC
possibly homozygous
51635945
10
45062523
45062524
A
AGAG
5
GENIC
heterozygous
51635946
10
45062710
45062711
A
G
19
GENIC
homozygous
51635947
10
45062865
45062869
TCTT
----
6
GENIC
heterozygous
51441661
10
45062888
45062889
T
TTC
3
GENIC
heterozygous
51441662
10
45063742
45063743
C
T
19
GENIC
possibly homozygous
51635950
10
45064763
45064764
C
T
23
GENIC
possibly homozygous
51635952
10
45065689
45065690
C
T
35
GENIC
possibly homozygous
51635953
10
45065758
45065759
A
C
20
GENIC
homozygous
51635954
10
45066802
45066803
G
A
11
GENIC
homozygous
51635957
10
45066885
45066886
A
AACTGAGCCTACACAAGATGACAGGTAAGCAG
1
GENIC
homozygous
52372836
10
45067181
45067182
C
T
22
GENIC
possibly homozygous
51635958
10
45068963
45068964
T
A
22
GENIC
possibly homozygous
51635960
10
45062826
45062827
C
-
3
GENIC
heterozygous
52317907
