chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
104584967
104584968
T
TGTATGTGGTGGTTACTGTCCAAGTA
20
GENIC
homozygous
45480785
X
104585192
104585193
A
G
16
GENIC
homozygous
45264083
X
104585193
104585194
G
T
15
GENIC
homozygous
45480787
X
104585197
104585198
C
CA
17
GENIC
homozygous
45189968
X
104585198
104585199
C
T
17
GENIC
homozygous
45480789
X
104585203
104585204
C
T
19
GENIC
homozygous
45189970
X
104585211
104585212
G
GT
23
GENIC
homozygous
45189971
X
104585213
104585214
G
GA
22
GENIC
homozygous
45189972
X
104585221
104585222
T
TC
22
GENIC
homozygous
45189973
X
104585237
104585238
T
G
21
GENIC
homozygous
45264084
X
104585239
104585240
C
G
22
GENIC
homozygous
45264085
X
104585242
104585243
A
T
22
GENIC
homozygous
45519563
X
104585243
104585244
A
ACC
23
GENIC
homozygous
45189974
X
104585246
104585247
G
T
24
GENIC
homozygous
45189975
X
104585248
104585249
G
T
23
GENIC
homozygous
45189976
