chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
165400091554000916GA25GENIChomozygous800663508
165400258154002582AG24GENIChomozygous800663509
165400352154003522AC35GENIChomozygous800663510
165400380954003810CT33GENIChomozygous800663511
165400726754007268TC27GENIChomozygous800663512
165400917354009174CA28GENIChomozygous800663513
165401112554011126AG17GENIChomozygous800663514
165401315054013151AG29GENICpossibly homozygous800663515
165401370254013703TA31GENIChomozygous800663516
165401524754015248TC38GENIChomozygous800663517
165401555654015557AG30GENIChomozygous800663518
165401822654018227AG34GENIChomozygous800663519
165402366154023662TC44GENIChomozygous800663520
165402504854025049AC16GENIChomozygous800663521
165402639454026395TG38GENIChomozygous800663522
165402646454026465CT42GENIChomozygous800663523
165402646854026469AG39GENIChomozygous800663524
165402800154028002GA32GENIChomozygous800663525
165402841554028416TC28GENIChomozygous800663526
165402851754028518CT34GENIChomozygous800663527
165402966954029670CT22GENIChomozygous800663528
165402970554029706CT20GENIChomozygous800663529