chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122272668422726685AC18GENIChomozygous115514645
122272676422726765GC20GENIChomozygous115514646
122272698622726987TC21GENIChomozygous115514647
122272709722727098AG10GENIChomozygous115514648
122272720722727208GA8GENIChomozygous115514649
122272728622727287AT18GENIChomozygous115514650
122272744922727450CT38GENIChomozygous115514651
122272775122727752GA12GENICpossibly homozygous115514652
122272826522728266AG18GENIChomozygous115514654
122272854022728541GA21GENIChomozygous115514655
122272870922728710GT32GENIChomozygous115514656
122272899322728994GA24GENIChomozygous115514657
122272915322729154CT24GENIChomozygous115514658
122272915622729157CT25GENIChomozygous115514659
122272671822726718TACA19GENIChomozygous131115187
122272718422727185GC8GENIChomozygous115421854
122273098322730984GT14GENIChomozygous115514660