chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101421707914217080A-26GENICheterozygous51622874
101421825814218259TG21GENICheterozygous51622875
101421860014218601TC29GENICpossibly homozygous51329145
101421947314219474AG19GENICheterozygous51622877
101421964814219649AT20GENICheterozygous51622878
101421978914219790TC29GENICheterozygous51622879
101422006114220062TC34GENICheterozygous51622880
101422119314221194TC22GENICheterozygous51622881
101422709614227097TC4GENICheterozygous51622890
101422860314228604T-4GENICheterozygous51810364
101422868814228689GT8GENICheterozygous51810368
101422932814229329TG22GENICheterozygous51622896