chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
116059955
116059956
C
CA
8
GENIC
possibly homozygous
45727517
X
116059955
116059956
C
CAA
8
GENIC
heterozygous
45727518
X
116059975
116059976
C
A
11
GENIC
homozygous
45200601
X
116060012
116060014
TT
--
3
GENIC
heterozygous
45200602
X
116060013
116060014
T
-
3
GENIC
heterozygous
45598161
X
116060596
116060597
A
AGTGTGTGTGTGTGTGT
8
GENIC
heterozygous
45788916
X
116060601
116060605
GTGT
----
8
GENIC
heterozygous
45522227
X
116060603
116060605
GT
--
8
GENIC
heterozygous
45817832
X
116062520
116062521
A
ATG
16
GENIC
homozygous
45817833
X
116062673
116062674
T
TGTGCTTGTGTGTGTGTGTGTGTGTGTGTGTTCATATGAGTAC
5
GENIC
heterozygous
45889534
X
116064252
116064253
T
C
18
GENIC
homozygous
45200612
X
116064948
116064949
C
CGTGTGT
2
GENIC
homozygous
45797666
X
116065151
116065152
A
ATG
5
GENIC
homozygous
45481652
X
116065411
116065412
A
-
9
GENIC
homozygous
45727522
X
116066902
116066903
G
GAC
7
GENIC
heterozygous
45634437
X
116066904
116066905
G
GAC
9
GENIC
possibly homozygous
45817834
