chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1541412774141278T14GENIChomozygous403369592
1541412774141278TG14GENICheterozygous403369593
1541596504159651A12GENIChomozygous403656598
1541596504159651AT12GENICheterozygous403656599
1541596554159656CT13GENIChomozygous403656602
1541596554159656C13GENICheterozygous403656603
1541596614159662C13GENICheterozygous403656604
1541596614159662CT13GENICpossibly homozygous139654078