chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84862645348626454TC39GENIChomozygous117002501
84862649948626500GA42GENIChomozygous117002503
84862661448626615AT48GENIChomozygous117002505
84862669748626698GA44GENIChomozygous117002507
84862724948627250CA49GENICpossibly homozygous117002509
84862849248628493GA41GENIChomozygous117002511
84862921748629218CT43GENIChomozygous117002513
84862974848629749GA60GENIChomozygous117002515
84863203048632031TC65GENIChomozygous117002517
84863247548632476TG46GENIChomozygous117002519
84863287448632875CT32GENIChomozygous117002521
84863355448633555CA55GENIChomozygous116957252
84863278148632782GA38GENIChomozygous116957250
84863436248634363AG31GENIChomozygous116957254
84863471648634717TC46GENIChomozygous116957258
84863486648634867AG48GENIChomozygous116957260
84863568848635689TC48GENIChomozygous116957262
84863622748636228CG49GENICpossibly homozygous117002523
84863582448635827TCC41GENIChomozygous132122116