chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115149584115149585TA25GENICpossibly homozygous112814463
4115151701115151702GA35GENIChomozygous112814465
4115152658115152659TC45GENIChomozygous112814467
4115152904115152905TG50GENICpossibly homozygous112814469
4115153961115153962CT31GENIChomozygous112814471