chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
10544258
10544259
A
G
19
GENIC
homozygous
51324887
10
10544345
10544346
G
T
16
GENIC
homozygous
51324888
10
10544683
10544687
TATT
----
4
GENIC
homozygous
51324889
10
10544789
10544790
G
A
15
GENIC
homozygous
51324890
10
10546506
10546508
AC
--
12
GENIC
possibly homozygous
51324896
10
10547269
10547270
A
C
19
GENIC
possibly homozygous
51324897
10
10548179
10548180
G
A
16
GENIC
possibly homozygous
51324898
10
10549415
10549416
A
G
11
GENIC
possibly homozygous
51324901
10
10551594
10551595
T
G
19
GENIC
homozygous
51324902
10
10551973
10551974
A
G
11
GENIC
possibly homozygous
51324903
10
10555864
10555865
C
T
22
GENIC
possibly homozygous
51324904
10
10556971
10556972
A
G
27
GENIC
possibly homozygous
51324905
10
10557208
10557209
A
G
11
GENIC
heterozygous
51324906
10
10559060
10559061
A
G
16
GENIC
possibly homozygous
51324907
10
10560108
10560110
TG
--
17
GENIC
possibly homozygous
51324908
10
10560404
10560405
G
GTGTGCATGCACATGCACATGCACA
3
GENIC
heterozygous
51324909
