chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129790133129790134AG32GENIChomozygous54109579
7129791161129791162TTG23GENICpossibly homozygous54109580
7129791273129791274GA27GENIChomozygous54109581
7129791328129791329GT36GENIChomozygous54109582
7129792326129792327GA33GENIChomozygous54109583
7129793490129793491CT41GENIChomozygous54109584
7129793818129793819AG30GENIChomozygous54109585
7129793994129793995TC24GENIChomozygous54109586