chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1541412774141278T18GENICpossibly homozygous403369592
1541412774141278TG18GENICheterozygous403369593
1541596504159651A12GENICheterozygous403656598
1541596504159651AT12GENICheterozygous403656599
1541596534159654CT14GENICheterozygous403369594
1541596534159654C14GENICheterozygous403369595
1541596554159656CT14GENICheterozygous403656602
1541596554159656C14GENICheterozygous403656603
1541596594159660CT15GENICheterozygous140916828
1541596594159660C15GENICheterozygous403369598
1541596594159660CA15GENICheterozygous403369599
1541596614159662C15GENICheterozygous403656604
1541596614159662CT15GENICheterozygous139654078