chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403357914033583TTTT----21GENICpossibly homozygous51622641
101403358014033583TTT---21GENICheterozygous51622642
101403360314033604CCT33GENICpossibly homozygous51622643
101403406114034062TC56GENIChomozygous51622644
101403420714034208AAAT40GENIChomozygous51622645
101403433814034339A-43GENIChomozygous51622646
101403462714034628GA52GENICpossibly homozygous51622647
101403486914034870CA44GENIChomozygous51622648
101403531614035318AA--1GENIChomozygous51622649
101403675914036760A-26GENIChomozygous51622650
101403733314037334GC57GENIChomozygous51622651
101403920514039206TC47GENIChomozygous51622652
101404104614041052GTGTGT------8GENIChomozygous51622653
101404107314041074TTG21GENICheterozygous51622654
101404375314043754AG54GENIChomozygous51622655
101404423614044237TC68GENIChomozygous51622656
101404493714044941TTTG----53GENIChomozygous51622657
101404532914045330GA52GENIChomozygous51622658
101404540014045401TTTCCTGGGAGC24GENIChomozygous51622659