chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8128022891128022891T28GENICpossibly homozygous128646864
8128023611128023612CT21GENIChomozygous116720047
8128023644128023645CA30GENIChomozygous116720049
8128024025128024025C24GENICpossibly homozygous128646865
8128024905128024906CT27GENIChomozygous116720053
8128025219128025220TC30GENIChomozygous116720055
8128025235128025236AG29GENIChomozygous116720057
8128025502128025503GA34GENIChomozygous116720059
8128025523128025524TC30GENIChomozygous116720061
8128026828128026829TC21GENIChomozygous116720063
8128026900128026901AT23GENIChomozygous116720065
8128026933128026934TC26GENIChomozygous116720067
8128024413128024414TC40GENIChomozygous117072044