chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
15155445
15155446
T
C
19
GENIC
homozygous
108233146
X
15156375
15156376
T
C
29
GENIC
homozygous
108233148
X
15157718
15157719
G
T
43
GENIC
homozygous
108233150
X
15158284
15158285
T
C
44
GENIC
homozygous
108233152
X
15159359
15159360
G
A
25
GENIC
homozygous
108233154
X
15157523
15157525
AC
33
GENIC
homozygous
129722486
X
15158562
15158562
TAAAAAGTAGATGGGGGCTGGAGAGATGGCTCAGCCGTTAAAGGCTAGGCTCACAACCAAAAATA
29
GENIC
homozygous
129722487
X
15159941
15159942
C
19
GENIC
homozygous
129722488
X
15159951
15159952
G
20
GENIC
homozygous
129722489
X
15159963
15159964
C
G
19
GENIC
homozygous
108562904
X
15160002
15160003
G
T
24
GENIC
homozygous
108562906
X
15160028
15160029
T
G
25
GENIC
homozygous
108562908
X
15160146
15160147
T
C
37
GENIC
homozygous
108562910
X
15160038
15160039
T
C
27
GENIC
homozygous
108653870
X
15160088
15160089
T
C
35
GENIC
homozygous
108439110
X
15162188
15162189
C
T
36
GENIC
homozygous
108233156
X
15162522
15162523
G
30
GENIC
homozygous
129722490
X
15163758
15163759
C
T
30
GENIC
homozygous
108233158
X
15162029
15162030
T
C
23
GENIC
homozygous
119905735
X
15162039
15162040
G
A
23
GENIC
homozygous
119905736
