chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2165077095165077096GC11GENIChomozygous110112210
2165077868165077869GA14GENIChomozygous120375689
2165077986165077987GA8GENIChomozygous110112212
2165078450165078451TC12GENIChomozygous110112213
2165078511165078512TC11GENIChomozygous110112214
2165080417165080418CT15GENICpossibly homozygous120375690
2165080847165080848AG13GENIChomozygous110112216
2165081069165081070CA20GENIChomozygous110112217
2165081420165081421AG26GENIChomozygous110112218
2165083601165083602AG19GENIChomozygous110895800
2165083626165083627CG23GENIChomozygous120375691
2165083643165083644CG24GENIChomozygous110895802
2165083652165083653TG23GENIChomozygous110895803
2165083698165083699TG21GENIChomozygous110895805
2165083772165083773AG15GENIChomozygous110895807