chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403406114034062TC10GENIChomozygous51622644
101403420714034208AAAT10GENIChomozygous51622645
101403433814034339A-7GENIChomozygous51622646
101403462714034628GA13GENIChomozygous51622647
101403675914036760A-9GENIChomozygous51622650
101403733314037334GC15GENIChomozygous51622651
101403920514039206TC11GENIChomozygous51622652
101404375314043754AG10GENIChomozygous51622655
101404423614044237TC23GENIChomozygous51622656
101404493714044941TTTG----12GENIChomozygous51622657
101404532914045330GA21GENIChomozygous51622658