chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58259056782590568CT22GENIChomozygous113896043
58259332982593330AG21GENIChomozygous113896045
58259342782593428AT25GENIChomozygous113896046
58259353082593531GA21GENIChomozygous113896047
58259359682593597CA24GENIChomozygous113896048
58259377682593777AG21GENIChomozygous113896049
58259424282594243TC36GENICpossibly homozygous113896050
58259472582594726TC29GENIChomozygous113896051
58259489882594899GA25GENIChomozygous113896052
58259500782595008AG23GENIChomozygous113896053
58259519182595192TC30GENIChomozygous113896054
58259532682595327AC30GENIChomozygous113896055
58259674282596743GT17GENIChomozygous113896056
58259679782596798CT14GENIChomozygous113896057
58259694582596946TC23GENIChomozygous113896058
58259706882597069TC25GENIChomozygous113896059
58259815982598160CT25GENIChomozygous113896060
58260054882600549TG27GENIChomozygous113896061
58260103082601031AT13GENIChomozygous113896062