chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71030411110304112GT26GENIChomozygous68593285
71030782110307822AT40GENICpossibly homozygous68593295
71030901510309016CT36GENIChomozygous68593297
71030966410309665TG35GENIChomozygous68593299
71031015010310151TC30GENIChomozygous68593302
71031176810311769GA42GENIChomozygous68593304
71031283410312835CT45GENIChomozygous68593306
71031459510314596AG26GENIChomozygous68593308
71031757310317574CT50GENIChomozygous68593310
71031804910318050AG35GENIChomozygous68593312
71031819010318191GA32GENIChomozygous68593316
71031873210318733CA32GENIChomozygous68593318
71031878010318781CT28GENIChomozygous68593320
71032013910320140TC24GENIChomozygous68593321
71032175810321759CG35GENIChomozygous68593323
71032176810321769CT35GENIChomozygous68593325
71032205010322051GT36GENIChomozygous68593327
71032219510322196AG38GENIChomozygous68593329
71032248710322488AG35GENIChomozygous68593331
71032419210324193AG34GENIChomozygous68593333
71032432010324321TC30GENIChomozygous68593335