chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4104416219104416219A25GENIChomozygous136909089
4104416949104416950G15GENIChomozygous136909090
4104418008104418009AT35GENIChomozygous137186365
4104418049104418050CT30GENIChomozygous137186366
4104419129104419130TC35GENIChomozygous137186367
4104419394104419395GA19GENIChomozygous137186368
4104420528104420540AGAAAGAGAGAA16GENIChomozygous136909091
4104420716104420717GA20GENICpossibly homozygous137186369