chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4116928349116928350CT4GENIChomozygous71110287
4116928393116928394GC5GENIChomozygous71110299
4116928409116928410AC17GENIChomozygous71110304
4116928435116928436CT3GENIChomozygous71110309
4116928518116928519GC20GENIChomozygous71110326
4116963142116963143TC19GENIChomozygous71110484
4116963153116963154CA18GENICpossibly homozygous71110488
4116974171116974172GA3GENIChomozygous71110558