chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5168546657168546658GA30GENIChomozygous56083018
5168546712168546713AT31GENICpossibly homozygous56083019
5168547964168547965GA28GENIChomozygous56083020
5168548403168548404AG32GENIChomozygous56083021
5168548454168548455AG28GENIChomozygous56083022
5168548628168548629GA39GENIChomozygous56083023
5168548659168548660TC41GENIChomozygous56083024
5168548703168548704GA34GENIChomozygous56083025
5168548980168548981GA23GENIChomozygous56083026
5168549022168549023CG21GENIChomozygous56083027
5168550078168550079GA36GENIChomozygous56083028
5168550914168550915CT72GENICheterozygous56083029
5168550918168550919AG72GENICpossibly homozygous56083030
5168550935168550936TC66GENICheterozygous56083031
5168551546168551547AG27GENIChomozygous56083032
5168551823168551824TC25GENIChomozygous56083033
5168551888168551889GA21GENIChomozygous56083034
5168552318168552319CT18GENIChomozygous56083035
5168553413168553414CT21GENICpossibly homozygous56083036
5168554722168554723A-31GENICheterozygous56083037
5168554724168554725C-30GENIChomozygous56083038
5168555161168555162AACC13GENIChomozygous56083039