chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
113000566
113000567
C
CTGTGTGTGTGTG
14
GENIC
heterozygous
45595060
X
113000567
113000569
TG
--
14
GENIC
heterozygous
45619290
X
113001632
113001634
TT
--
18
GENIC
homozygous
45197069
X
113001638
113001639
T
TGC
19
GENIC
homozygous
45197070
X
113001648
113001649
A
C
23
GENIC
homozygous
45197071
X
113001653
113001654
G
T
21
GENIC
homozygous
45197072
X
113001676
113001677
A
AGAG
20
GENIC
homozygous
45197073
X
113006153
113006154
C
T
32
GENIC
homozygous
45521080
X
113001678
113001679
A
AGAAGT
19
GENIC
homozygous
45521073
X
113001680
113001687
CACCCCC
-------
21
GENIC
homozygous
45521075
X
113001688
113001689
C
T
20
GENIC
homozygous
45521077
X
113006159
113006160
A
G
25
GENIC
possibly homozygous
45197075
X
113006173
113006174
A
AC
26
GENIC
homozygous
45197076
X
113008983
113008984
G
GT
5
GENIC
heterozygous
45595068
X
113020742
113020743
C
CATGT
17
GENIC
possibly homozygous
45197077
X
113020742
113020743
C
CCCGT
17
GENIC
heterozygous
45311789
X
113022240
113022241
G
GT
15
GENIC
heterozygous
45197078
X
113022240
113022241
G
GTT
15
GENIC
heterozygous
45264863
X
113025705
113025707
AC
--
11
GENIC
possibly homozygous
45550712
X
113029087
113029089
AC
--
2
GENIC
homozygous
45573193
X
113032671
113032672
T
TTTGCCCGGAAACCGGGAAAGGGAATAACACTCGAAATGTATACAAGAAATACTCAAGTTAATAAAAAAAA
11
GENIC
homozygous
45481356
X
113039630
113039631
C
CT
10
GENIC
homozygous
45197079
X
113042986
113042987
T
TC
13
GENIC
homozygous
45197080
X
113059722
113059724
AC
--
3
GENIC
heterozygous
45521082
X
113060883
113060884
C
-
14
GENIC
homozygous
45481358
X
113065197
113065203
ACACAC
------
5
GENIC
heterozygous
45595082
X
113065201
113065203
AC
--
5
GENIC
heterozygous
45595084
X
113071924
113071926
CT
--
13
GENIC
heterozygous
45595088
X
113073023
113073035
GAGAGAGAGAGA
------------
7
GENIC
heterozygous
45521084
X
113082299
113082300
C
CGGTTAGGGGGATTTTGGTCTGGAAACAGGGAAG
2
GENIC
homozygous
45521088
