chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
71350485
71350486
T
G
18
GENIC
possibly homozygous
45893633
X
71352273
71352274
G
T
19
GENIC
homozygous
45260073
X
71356308
71356316
TCTTTCTT
--------
1
GENIC
homozygous
45511836
X
71361083
71361087
GTGT
----
2
GENIC
homozygous
45511838
X
71372026
71372027
A
G
20
GENIC
homozygous
45260118
X
71377390
71377392
AC
--
3
GENIC
heterozygous
45588199
X
71372027
71372028
G
T
20
GENIC
homozygous
45478617
X
71372039
71372040
A
-
19
GENIC
homozygous
45146764
X
71372044
71372045
A
AG
18
GENIC
homozygous
45146765
X
71372771
71372772
T
C
14
GENIC
homozygous
45146766
X
71387976
71387978
GT
--
9
GENIC
heterozygous
45633476
X
71396407
71396409
CA
--
8
GENIC
heterozygous
45511844
X
71396459
71396461
AC
--
8
GENIC
heterozygous
45260145
X
71397065
71397066
A
AG
13
GENIC
homozygous
45146773
X
71397944
71397945
G
-
3
GENIC
heterozygous
45478621
X
71401900
71401901
G
T
19
GENIC
homozygous
45146774
X
71405803
71405804
C
CA
14
GENIC
heterozygous
45613106
X
71406965
71406966
C
CGT
1
GENIC
homozygous
45547638
X
71408511
71408512
T
-
6
GENIC
heterozygous
45569734
X
71418177
71418207
TGGAAGCAACCCCCAGTGTTGCTGATTATG
------------------------------
8
GENIC
homozygous
45511848
X
71424548
71424555
GTTGATG
-------
8
GENIC
heterozygous
45588201
X
71424591
71424600
ATGAAGCCT
---------
18
GENIC
heterozygous
45146777
X
71429432
71429433
A
ATG
7
GENIC
heterozygous
45260191