chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221504747221504748CT20GENICpossibly homozygous62589536
1221508190221508191CT11GENICpossibly homozygous61094033
1221510285221510286TA24GENICpossibly homozygous61094036
1221510672221510673T-10GENIChomozygous62445191
1221511993221511994AG15GENIChomozygous61094039
1221513366221513367TC16GENIChomozygous61094040
1221514210221514211TC15GENICpossibly homozygous61094041
1221515199221515200AG19GENIChomozygous61094042