chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145119403145119404TA30GENIChomozygous112870628
4145119523145119524GC23GENIChomozygous112870629
4145119998145119999TC13GENIChomozygous112870630
4145121025145121026CT18GENICpossibly homozygous112870631
4145121086145121087CT15GENIChomozygous112870632
4145121377145121378GA32GENIChomozygous112870633
4145123158145123159TC24GENIChomozygous112870634
4145123623145123624GT33GENIChomozygous112870635
4145124114145124115AG17GENIChomozygous112870636
4145125968145125969CT25GENIChomozygous112870637
4145126827145126828CT26GENIChomozygous112870638
4145146498145146499AG3GENIChomozygous112870642