chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X104720548104720549AG11GENIChomozygous518638666
X104721477104721478GA7GENIChomozygous518638667
X104723788104723789AG9GENIChomozygous518638668
X104724149104724150GT7GENICheterozygous518638669
X104727044104727045A-13GENIChomozygous690077792
X104728161104728162G-12GENIChomozygous690077793
X104728227104728228CT14GENIChomozygous518638670
X104730133104730134T-7GENIChomozygous690077795
X104730149104730150TC8GENICpossibly homozygous518638671
X104731410104731411GT13GENICheterozygous518638672
X104731568104731569CT6GENIChomozygous518638673
X104733371104733372GA7GENIChomozygous518638674
X104734161104734162GGC8GENICpossibly homozygous690077796