chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
71340092
71340093
C
CCCAG
5
GENIC
heterozygous
45803725
X
71340094
71340095
C
CT
4
GENIC
heterozygous
45803727
X
71357915
71357918
AAA
---
5
GENIC
heterozygous
45260090
X
71372026
71372027
A
G
12
GENIC
homozygous
45260118
X
71377390
71377392
AC
--
4
GENIC
heterozygous
45588199
X
71381701
71381703
GT
--
5
GENIC
heterozygous
45511842
X
71357917
71357918
A
-
5
GENIC
heterozygous
45695687
X
71361085
71361087
GT
--
2
GENIC
heterozygous
45569728
X
71372027
71372028
G
T
13
GENIC
homozygous
45478617
X
71372039
71372040
A
-
7
GENIC
homozygous
45146764
X
71372044
71372045
A
AG
8
GENIC
homozygous
45146765
X
71372771
71372772
T
C
20
GENIC
homozygous
45146766
X
71396407
71396409
CA
--
5
GENIC
heterozygous
45511844
X
71397065
71397066
A
AG
9
GENIC
homozygous
45146773
X
71397944
71397945
G
-
7
GENIC
heterozygous
45478621
X
71401900
71401901
G
T
12
GENIC
homozygous
45146774
X
71418177
71418207
TGGAAGCAACCCCCAGTGTTGCTGATTATG
------------------------------
9
GENIC
homozygous
45511848
X
71429432
71429433
A
ATG
8
GENIC
heterozygous
45260191
X
71429432
71429433
A
ATGTGTGTGTGTGTGTGTGTG
8
GENIC
heterozygous
45588203
