chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891244518912446CT24GENICheterozygous51337771
101891245118912453TG--25GENICheterozygous51337772
101891594218915943AG37GENICheterozygous51337801
101891599818915999TC19GENICheterozygous51337802
101892033818920339GA36GENICheterozygous51337825
101892060318920604GC38GENICheterozygous51337826
101892080118920802GC50GENICheterozygous51337827
101892086518920866GA37GENICheterozygous51337828
101892100418921005TC25GENICheterozygous51337829
101892103418921035CT15GENICheterozygous51337830
101892107118921072CT6GENICheterozygous51337831
101892151518921516CT28GENICheterozygous51337836
101892157118921572TC33GENICheterozygous51337837
101892167318921674T-23GENICheterozygous51337838