chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85927826359278264CT49GENIChomozygous117108127
85927947659279477AC41GENIChomozygous116511374
85927960159279602GA43GENIChomozygous117108128
85927970959279710AG43GENIChomozygous116511376
85927987959279880GA34GENIChomozygous116511378
85928055159280552CT43GENIChomozygous116511382
85928096459280965GA42GENIChomozygous116511384
85928110259281103AG43GENIChomozygous117108129
85928505459285055AC40GENIChomozygous116511388
85928162859281628TG34GENIChomozygous132122489
85928250659282509CTT43GENIChomozygous132122490
85928568759285688TG40GENICpossibly homozygous117108130
85928603459286035AC45GENIChomozygous117108131
85928623059286231C36GENIChomozygous132122491
85928762659287627GA14GENICpossibly homozygous116831173
85928773059287731AG34GENIChomozygous116511390
85928810359288104AC52GENIChomozygous116511392
85928815559288156TC50GENIChomozygous116511394
85929006559290081GCAGCTGGAGTTCCGG47GENIChomozygous132122492
85929172459291725AG42GENIChomozygous116511398
85929176659291767TC48GENIChomozygous116511400
85929369759293698CT40GENIChomozygous117108133