chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10102136651102136652GA14GENIChomozygous116712602
10102136666102136667TC13GENIChomozygous116712604
10102138186102138187CG5GENIChomozygous116712606
10102138273102138274CT22GENIChomozygous116712608
10102138431102138432CA12GENIChomozygous116712610
10102138625102138626CG8GENIChomozygous116712612
10102138627102138628GA8GENIChomozygous116712614
10102138634102138635GC7GENIChomozygous116712616
10102138638102138639GA11GENIChomozygous116712618
10102138958102138959GA5GENICheterozygous126465566
10102138973102138974CT10GENIChomozygous116712622
10102140833102140834TC22GENIChomozygous116712626
10102140843102140844AC22GENIChomozygous116712628
10102140973102140974TG5GENICheterozygous117232363