chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145119403145119404TA52GENIChomozygous112870628
4145119523145119524GC52GENIChomozygous112870629
4145119998145119999TC51GENIChomozygous112870630
4145121025145121026CT70GENIChomozygous112870631
4145121086145121087CT58GENIChomozygous112870632
4145121377145121378GA61GENIChomozygous112870633
4145123158145123159TC39GENIChomozygous112870634
4145123623145123624GT55GENIChomozygous112870635
4145124114145124115AG38GENIChomozygous112870636
4145125968145125969CT64GENICpossibly homozygous112870637
4145126827145126828CT66GENIChomozygous112870638
4145127769145127770GT39GENIChomozygous112870639
4145142820145142821AG39GENIChomozygous112870640
4145146498145146499AG40GENIChomozygous112870642