chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8110604182110604183CA42GENIChomozygous52802111
8110604482110604483CG31GENIChomozygous52802113
8110604804110604805AG38GENIChomozygous52802115
8110604922110604923AC51GENIChomozygous52802117
8110605131110605132CT37GENIChomozygous52802119
8110605180110605181CT31GENIChomozygous52802121
8110605702110605703TC25GENIChomozygous52802123
8110606000110606001CT37GENIChomozygous52802125
8110606443110606444GGCACA5GENICheterozygous52802127
8110606443110606444GGCA5GENICheterozygous53034411
8110607345110607346GA31GENIChomozygous52802129
8110607973110607974GGTTTT23GENIChomozygous52802130
8110608350110608354GTGT----19GENICheterozygous52802134
8110608352110608354GT--19GENICheterozygous52802136
8110609470110609471AAG34GENIChomozygous52802138
8110609478110609479GT34GENIChomozygous52802140
8110612611110612612GA28GENIChomozygous52802142
8110613628110613629TTC31GENIChomozygous52802144
8110614033110614034GA38GENIChomozygous53164394
8110614289110614290AG36GENIChomozygous52802146
8110614667110614668AG49GENIChomozygous52802148
8110614837110614838CT43GENIChomozygous52802150
8110614881110614882CG40GENIChomozygous52802152
8110614884110614885AG37GENIChomozygous52802154
8110615410110615411GGC22GENIChomozygous52802156
8110615905110615906GC38GENICpossibly homozygous52802158
8110616387110616388TC47GENIChomozygous52802160