chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
3125189
3125190
C
T
13
GENIC
heterozygous
53768174
7
3125189
3125190
C
CCT
11
GENIC
homozygous
53768176
7
3125341
3125342
G
A
31
GENIC
homozygous
53768178
7
3125872
3125876
GTGT
----
8
GENIC
heterozygous
53768179
7
3125874
3125876
GT
--
8
GENIC
heterozygous
53768181
7
3125911
3125912
T
C
33
GENIC
possibly homozygous
53768183
7
3125921
3125922
T
C
36
GENIC
possibly homozygous
53768185
7
3127415
3127440
CAGATCGTCTAGGATGGGAGCTACA
-------------------------
7
GENIC
homozygous
53768187
7
3128151
3128152
A
ACACAGGGAGATCCCTGGGCT
19
GENIC
homozygous
53768189
7
3128155
3128156
T
A
34
GENIC
heterozygous
53768191
7
3128656
3128657
C
G
45
GENIC
homozygous
53768193
7
3129301
3129303
GG
--
5
GENIC
heterozygous
53768195
7
3131429
3131430
C
T
53
GENIC
homozygous
53768199