chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
114774738
114774739
G
-
27
GENIC
homozygous
45197738
X
114775428
114775429
G
C
40
GENIC
homozygous
45197739
X
114775656
114775657
T
TCAGA
7
GENIC
homozygous
45873205
X
114775695
114775696
G
GAAAGACAC
23
GENIC
homozygous
45772818
X
114775908
114775909
C
CCCT
14
GENIC
homozygous
45197741
X
114776612
114776613
G
A
26
GENIC
homozygous
45197742
X
114776823
114776824
C
G
14
GENIC
homozygous
45197743
X
114776916
114776917
C
T
19
GENIC
homozygous
45197744
X
114777235
114777236
G
T
21
GENIC
homozygous
45197745
X
114777722
114777723
T
C
27
GENIC
homozygous
45197746
X
114778190
114778191
C
T
13
GENIC
homozygous
45197747
X
114778379
114778385
GTGTGT
------
10
GENIC
heterozygous
45521380
X
114781254
114781255
C
T
21
GENIC
homozygous
45197748
X
114781836
114781837
G
A
30
GENIC
homozygous
45197749
X
114782072
114782073
T
TA
26
GENIC
possibly homozygous
45197750
X
114782782
114782783
C
CCCGT
35
GENIC
homozygous
45197751
X
114783283
114783287
CCCC
----
12
GENIC
homozygous
45197752
X
114784366
114784367
C
CACCCTCCAGCCTGT
14
GENIC
homozygous
45481456
X
114787860
114787861
C
-
19
GENIC
heterozygous
45265003
X
114788098
114788099
A
G
21
GENIC
homozygous
45197759
X
114789750
114789752
CG
--
28
GENIC
homozygous
45197760
X
114790868
114790869
T
C
14
GENIC
homozygous
45197761
X
114791808
114791809
T
-
19
GENIC
homozygous
45197762
X
114794023
114794024
T
A
17
GENIC
homozygous
45197763
X
114794124
114794125
C
T
32
GENIC
homozygous
45197764
X
114794479
114794480
G
-
2
GENIC
homozygous
45197765
X
114794481
114794482
G
GT
5
GENIC
heterozygous
45197766
X
114794502
114794503
C
CCACTGTTTCTACATCGCCACCCACCGGGTCAAGCAGCAACAGGAAGAAGTCGT
3
GENIC
homozygous
45651234
