chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143616002236160023TG18GENICheterozygous49598134
143616031236160313TC26GENICheterozygous49598135
143616032036160321GA28GENICheterozygous49598136
143616033236160333TC25GENICheterozygous49598137
143617223136172232CT21GENIChomozygous48985055
143618601936186020AC21GENIChomozygous48659901
143618713436187135AG17GENIChomozygous48985063
143618735536187356TC13GENIChomozygous48985065
143618760136187602GA10GENIChomozygous48985067
143618772936187730GA15GENIChomozygous48985070
143618827036188271TC17GENIChomozygous48985071
143618847636188477TG17GENIChomozygous48985073
143618857336188574TC16GENIChomozygous48659905
143618881536188816TC11GENIChomozygous48659906
143618892336188924TA16GENIChomozygous48985075
143618892436188925TA16GENIChomozygous48985077
143619347636193477GA11GENIChomozygous48659909
143619649736196498TC24GENIChomozygous48659910
143619685236196853CG15GENIChomozygous48985079
143619975336199754CT15GENIChomozygous48985080
143620106936201070AG12GENIChomozygous48659913
143620228236202283CT16GENIChomozygous48985085
143620234136202342CT12GENIChomozygous48985087
143620493436204935CT24GENIChomozygous48659916
143620639236206393T-12GENIChomozygous48659917