chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1157175308157175309GA17GENIChomozygous74563328
1157175741157175742AG15GENICpossibly homozygous74563331
1157175883157175884AG19GENIChomozygous74563334
1157176060157176061GA18GENICpossibly homozygous74563337
1157176188157176189GT18GENIChomozygous74563340
1157176430157176431GA33GENIChomozygous74563343
1157176603157176604CT29GENIChomozygous75150208