chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1259812791259812792GT11GENICpossibly homozygous108626723
1259812814259812815AG13GENIChomozygous108626724
1259812834259812835AG13GENIChomozygous108626725
1259813229259813230TC8GENICheterozygous130241947
1259813242259813243GA6GENICheterozygous130241948
1259813243259813244CA6GENICheterozygous131799022
1259813428259813429GA1GENIChomozygous131799023
1259814568259814569AG2GENIChomozygous132385324
1259814527259814527CCATTTTGGCCAGATC5GENICheterozygous134781465
1259814528259814529AT5GENICheterozygous134798595
1259814530259814531AG5GENICheterozygous134798596