chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124363427843634279AG25GENIChomozygous115335411
124363439143634392GA22GENIChomozygous115335413
124363440743634408AT18GENIChomozygous115389569
124363457343634574GA29GENIChomozygous115335416
124363499443634995TC22GENIChomozygous115335418
124363525143635252TC20GENIChomozygous115335420
124363531343635314TC11GENIChomozygous115335422
124363543643635437GT15GENIChomozygous115335424
124363707743637078AT29GENIChomozygous115389571
124363745243637453CT22GENIChomozygous115335430
124363860743638608TA7GENIChomozygous115335432
124363917043639171GA13GENICpossibly homozygous115335434
124363946243639463GA19GENIChomozygous115335436
124364022343640224AG28GENIChomozygous115335440
124364048543640486TC26GENIChomozygous115335444
124364067243640673TC26GENIChomozygous115335446
124364078043640781TC26GENIChomozygous115335450