chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159955945699559456T18GENICpossibly homozygous139651109
159955976799559768C19GENIChomozygous139651110
159956027699560277AT12GENICheterozygous154913520
159956027699560277A12GENICheterozygous403387818
159956027899560279AT12GENICheterozygous140920260
159956028099560281AT12GENICheterozygous147614111
159956032299560323G12GENICheterozygous403387819
159956032299560323GA12GENICheterozygous403387820
159956081899560819TC27GENIChomozygous139812767
159956191399561914TC21GENIChomozygous139812768
159956200599562006CT16GENIChomozygous139812769
159956209399562094AC24GENIChomozygous139812770
159956209699562097AC25GENIChomozygous139812771
159956229599562296CT25GENIChomozygous142504584
159956295299562953TC17GENIChomozygous139812772
159956343999563440TC13GENIChomozygous139812773
159956380299563803TC31GENIChomozygous139812774
159956430899564309TC23GENIChomozygous139812775
159956464999564650GA25GENIChomozygous139812776
159956504799565048AG18GENIChomozygous139812777
159956514099565141GA14GENICpossibly homozygous139812778