chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18543863485438635CT20GENIChomozygous402951571
18543863485438635C20GENICheterozygous402951572
18543863685438637CG20GENICpossibly homozygous402951573
18543863685438637CT20GENICheterozygous402951574
18543863685438637C20GENICheterozygous402951575
18543863785438638CA20GENICpossibly homozygous402951576
18543863785438638C20GENICheterozygous402951577
18543864385438644CT19GENICpossibly homozygous402951580
18543864385438644C19GENICheterozygous402951581