chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143617223136172232CT20GENIChomozygous48985055
143618601936186020AC13GENICpossibly homozygous48659901
143618713436187135AG20GENIChomozygous48985063
143618735536187356TC8GENICpossibly homozygous48985065
143618760136187602GA21GENIChomozygous48985067
143618772936187730GA26GENICheterozygous48985070
143618827036188271TC15GENIChomozygous48985071
143618847636188477TG11GENICheterozygous48985073
143618857336188574TC12GENIChomozygous48659905
143618881536188816TC22GENIChomozygous48659906
143618892336188924TA24GENICheterozygous48985075
143618892436188925TA24GENICheterozygous48985077
143619347636193477GA5GENICheterozygous48659909
143619649736196498TC19GENICpossibly homozygous48659910
143619685236196853CG14GENIChomozygous48985079
143619975336199754CT10GENIChomozygous48985080
143620106936201070AG8GENICheterozygous48659913
143620228236202283CT18GENIChomozygous48985085
143620234136202342CT10GENIChomozygous48985087
143620493436204935CT11GENIChomozygous48659916
143620639236206393T-9GENIChomozygous48659917