chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
10544258
10544259
A
G
18
GENIC
homozygous
51324887
10
10544345
10544346
G
T
17
GENIC
homozygous
51324888
10
10544683
10544687
TATT
----
24
GENIC
homozygous
51324889
10
10544789
10544790
G
A
17
GENIC
homozygous
51324890
10
10545379
10545380
T
-
7
GENIC
homozygous
51324892
10
10545669
10545670
T
-
2
GENIC
homozygous
51324895
10
10546506
10546508
AC
--
26
GENIC
homozygous
51324896
10
10547269
10547270
A
C
23
GENIC
homozygous
51324897
10
10548179
10548180
G
A
18
GENIC
homozygous
51324898
10
10548818
10548819
C
T
11
GENIC
homozygous
51324899
10
10548836
10548837
T
A
13
GENIC
homozygous
51324900
10
10549415
10549416
A
G
23
GENIC
homozygous
51324901
10
10551594
10551595
T
G
18
GENIC
homozygous
51324902
10
10551973
10551974
A
G
34
GENIC
homozygous
51324903
10
10555864
10555865
C
T
29
GENIC
homozygous
51324904
10
10556971
10556972
A
G
22
GENIC
homozygous
51324905
10
10557208
10557209
A
G
23
GENIC
homozygous
51324906
10
10559060
10559061
A
G
29
GENIC
homozygous
51324907
10
10560108
10560110
TG
--
34
GENIC
homozygous
51324908
10
10560404
10560405
G
GTGTGCATGCACATGCACATGCACA
40
GENIC
homozygous
51324909