chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129790133129790134AG19GENIChomozygous54109579
7129791161129791162TTG12GENICpossibly homozygous54109580
7129791273129791274GA25GENIChomozygous54109581
7129791328129791329GT28GENIChomozygous54109582
7129792326129792327GA25GENIChomozygous54109583
7129793490129793491CT19GENIChomozygous54109584
7129793818129793819AG21GENIChomozygous54109585
7129793994129793995TC16GENIChomozygous54109586