chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129790133129790134AG29GENIChomozygous54109579
7129791161129791162TTG26GENICpossibly homozygous54109580
7129791273129791274GA52GENIChomozygous54109581
7129791328129791329GT48GENIChomozygous54109582
7129792326129792327GA46GENIChomozygous54109583
7129793490129793491CT57GENICpossibly homozygous54109584
7129793818129793819AG59GENIChomozygous54109585
7129793994129793995TC51GENIChomozygous54109586