chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129790133129790134AG6GENIChomozygous54109579
7129791161129791162TTG12GENICheterozygous54109580
7129791273129791274GA21GENIChomozygous54109581
7129791328129791329GT20GENICpossibly homozygous54109582
7129792326129792327GA18GENICpossibly homozygous54109583
7129793490129793491CT28GENICpossibly homozygous54109584
7129793818129793819AG13GENIChomozygous54109585
7129793994129793995TC20GENIChomozygous54109586