chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153871651153871652AG39GENICpossibly homozygous113398579
4153872809153872810AG22GENIChomozygous113398581
4153872908153872909GA45GENIChomozygous113398583
4153873329153873330TC42GENIChomozygous113398585
4153873342153873343AG44GENIChomozygous113398587
4153874885153874886AG46GENIChomozygous112890486
4153874951153874952TC35GENIChomozygous112890487
4153875760153875761GA39GENIChomozygous112890489
4153877410153877411TC34GENIChomozygous113398589
4153878243153878244TC43GENIChomozygous112890493
4153878862153878863AG40GENIChomozygous112890494
4153879296153879297GC38GENIChomozygous112890495