chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143615550036155501CCCAGGACCT1GENIChomozygous49283033
143617223136172232CT20GENIChomozygous48985055
143618601936186020AC16GENIChomozygous48659901
143618713436187135AG14GENIChomozygous48985063
143618735536187356TC6GENICheterozygous48985065
143618760136187602GA25GENIChomozygous48985067
143618772936187730GA29GENICpossibly homozygous48985070
143618827036188271TC22GENIChomozygous48985071
143618847636188477TG18GENICpossibly homozygous48985073
143618857336188574TC14GENIChomozygous48659905
143618881536188816TC16GENICpossibly homozygous48659906
143618892336188924TA9GENICheterozygous48985075
143618892436188925TA9GENICheterozygous48985077
143619347636193477GA10GENICheterozygous48659909
143619649736196498TC28GENIChomozygous48659910
143619685236196853CG14GENIChomozygous48985079
143619975336199754CT18GENIChomozygous48985080
143620106936201070AG12GENICheterozygous48659913
143620228236202283CT23GENIChomozygous48985085
143620234136202342CT16GENIChomozygous48985087
143620493436204935CT19GENIChomozygous48659916
143620639236206393T-3GENICheterozygous48659917