chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4180967959180967960GT109GENICheterozygous113069073
4180967986180967987GT143GENICheterozygous112975954
4180967996180967997CT145GENICheterozygous112975955
4180968019180968020CA127GENICheterozygous112975956
4180968024180968025AG124GENICheterozygous112975957
4180968025180968026TC125GENICheterozygous112975958
4180968029180968030GT128GENICheterozygous112975959
4180968032180968033AG130GENICheterozygous112975960
4180968045180968046AT166GENICheterozygous112975961
4180968059180968060GA165GENICheterozygous112975962
4180968060180968061TA165GENICheterozygous112975963
4180968082180968083CT148GENICheterozygous112975964
4180968087180968088CT140GENICheterozygous112975965
4180968094180968095TC128GENICheterozygous113069074
4180968095180968096GA126GENICheterozygous113069075
4180968104180968105TC124GENICheterozygous113069076