chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98142731081427311GA29GENICpossibly homozygous117585125
98142766581427666TG41GENIChomozygous117585129
98142833181428332AG18GENIChomozygous117585135
98142834081428341CA18GENIChomozygous117585137
98142874681428747TC18GENIChomozygous117848969
98142930581429306GT33GENIChomozygous117585143
98142934281429343TC32GENIChomozygous117585145
98143034781430348TC25GENIChomozygous117585149