chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
27421821
27421822
T
A
5
GENIC
homozygous
45113693
X
27421967
27421968
T
-
6
GENIC
homozygous
45378044
X
27422192
27422193
C
T
8
GENIC
homozygous
45113694
X
27423382
27423383
G
GCTAGGTGATTTTCATCAGTCTAGGTATAACTCCGTCATAAGTGAAGGAGCAT
18
GENIC
homozygous
45504437
X
27423387
27423388
G
GTAATATGCACTGTTTGT
19
GENIC
homozygous
45475550
X
27423398
27423399
G
GA
21
GENIC
homozygous
45113697
X
27425552
27425553
C
-
2
GENIC
heterozygous
45113698
X
27425872
27425873
G
C
4
GENIC
homozygous
45113703
X
27425886
27425887
T
A
6
GENIC
homozygous
45113705
X
27425888
27425889
A
T
7
GENIC
homozygous
45113706
X
27425890
27425891
A
T
7
GENIC
homozygous
45113707
X
27425972
27425973
G
C
16
GENIC
homozygous
45113708
X
27426308
27426309
A
G
17
GENIC
homozygous
45378052
X
27426368
27426369
T
C
17
GENIC
homozygous
45378054
X
27426374
27426375
C
A
17
GENIC
homozygous
45378056
X
27426600
27426604
GTGG
----
9
GENIC
homozygous
45113709
X
27427271
27427272
A
G
10
GENIC
homozygous
45113711
X
27427604
27427605
G
A
19
GENIC
homozygous
45378058
X
27427609
27427610
G
A
17
GENIC
homozygous
45378060
X
27427698
27427699
G
T
21
GENIC
homozygous
45378062
X
27427932
27427933
C
T
21
GENIC
homozygous
45378064
X
27428067
27428068
C
T
18
GENIC
homozygous
45113712
X
27428422
27428423
G
A
24
GENIC
homozygous
45113713
X
27429050
27429051
A
G
14
GENIC
homozygous
45113714
X
27430186
27430187
T
A
11
GENIC
homozygous
45378066
X
27430187
27430188
C
A
11
GENIC
homozygous
45378068
X
27430366
27430367
A
C
10
GENIC
homozygous
45113716
X
27430878
27430879
C
T
18
GENIC
homozygous
45113717
X
27431411
27431412
A
G
15
GENIC
homozygous
45113718
X
27432879
27432880
A
-
6
GENIC
homozygous
45378070
X
27433841
27433842
G
C
15
GENIC
homozygous
45113720
X
27434070
27434071
A
AT
7
GENIC
heterozygous
45113721
X
27434070
27434071
A
ATT
7
GENIC
possibly homozygous
45324160
X
27436402
27436403
T
G
4
GENIC
homozygous
45378072
