chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71030782110307822AT14GENIChomozygous68593295
71030901510309016CT24GENIChomozygous68593297
71030966410309665TG30GENIChomozygous68593299
71031015010310151TC15GENIChomozygous68593302
71031176810311769GA33GENIChomozygous68593304
71031283410312835CT18GENIChomozygous68593306
71031459510314596AG25GENIChomozygous68593308
71031757310317574CT24GENIChomozygous68593310
71031804910318050AG28GENIChomozygous68593312
71031819010318191GA23GENIChomozygous68593316
71031873210318733CA27GENIChomozygous68593318
71031878010318781CT21GENICpossibly homozygous68593320
71032013910320140TC14GENIChomozygous68593321
71032175810321759CG17GENIChomozygous68593323
71032176810321769CT13GENIChomozygous68593325
71032205010322051GT14GENIChomozygous68593327
71032219510322196AG18GENIChomozygous68593329
71032248710322488AG10GENIChomozygous68593331
71032419210324193AG22GENIChomozygous68593333
71032432010324321TC20GENIChomozygous68593335