chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155465443155465444GA18GENIChomozygous667262617
5155466069155466071AA--19GENIChomozygous767485673
5155466809155466810GT37GENIChomozygous667262618
5155466850155466851TG38GENIChomozygous667262619
5155466955155466956CG27GENICpossibly homozygous667262620
5155467079155467080A-26GENIChomozygous767485675
5155467099155467100CT31GENIChomozygous667262621
5155467380155467381GT15GENIChomozygous667262622
5155467579155467580CA11GENIChomozygous667262623
5155467674155467675CA16GENIChomozygous667262624
5155467756155467757TC20GENIChomozygous667262625
5155467773155467774GA24GENIChomozygous667262626
5155467820155467821AG22GENIChomozygous667262627
5155468002155468003AG21GENIChomozygous667262628