chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98840751888407519CA32GENICpossibly homozygous117383368
98841798488417985GA29GENICheterozygous117596605
98842762688427627GT20GENIChomozygous117383369
98844777588447776GT3GENIChomozygous117596607
98844778488447785GA7GENIChomozygous117383370
98844780388447804TG16GENIChomozygous117383371