chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3111023184111023185CT15GENICpossibly homozygous112292619
3111027093111027094AG23GENIChomozygous112292621
3111030487111030488CA33GENIChomozygous112292624
3111032427111032428TC20GENIChomozygous111673715
3111032781111032782GA19GENIChomozygous112292626
3111032903111032904CT25GENIChomozygous112292628
3111033085111033086CT19GENIChomozygous112292630
3111033907111033908CT21GENIChomozygous112292632
3111034780111034781TC18GENIChomozygous111673718
3111035679111035680TC30GENIChomozygous111673724
3111036221111036222AT24GENIChomozygous111673727