chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
730977573097758A-21GENICpossibly homozygous770997077
730978133097814A-29GENICpossibly homozygous770997078
730990873099088TC20GENIChomozygous674814887
731001163100117CCTG16GENIChomozygous770997079
731001393100140GGT20GENIChomozygous770997080
731001443100145CCG20GENIChomozygous770997081
731001503100151CCG18GENIChomozygous770997082
731002053100206CCAACA31GENIChomozygous770997083
731019813101982GA28GENICpossibly homozygous674814888
731031993103200GT18GENIChomozygous674814889
731048093104810TTG5GENICheterozygous770997085
731051303105131TC16GENIChomozygous674814890