chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891244518912446CT36GENICheterozygous51337771
101891245118912453TG--36GENICheterozygous51337772
101891594218915943AG36GENICheterozygous51337801
101891599818915999TC30GENICheterozygous51337802
101892033818920339GA46GENICheterozygous51337825
101892060318920604GC56GENICheterozygous51337826
101892080118920802GC57GENICheterozygous51337827
101892086518920866GA39GENICheterozygous51337828
101892100418921005TC27GENICheterozygous51337829
101892103418921035CT23GENICheterozygous51337830
101892107118921072CT18GENICheterozygous51337831
101892151518921516CT33GENICheterozygous51337836
101892157118921572TC44GENICheterozygous51337837
101892167318921674T-57GENICheterozygous51337838