chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103889217938892180AG10GENICheterozygous51421945
103889231338892314TC8GENIChomozygous51421946
103889233438892335T-3GENIChomozygous53139199
103889254938892550CA17GENIChomozygous51421947
103889280038892801TC20GENIChomozygous53139201
103889344138893442GC20GENIChomozygous53139203
103889390838893909TC11GENICheterozygous51421948
103889444038894441CT20GENICpossibly homozygous52876030
103889467738894678GA18GENIChomozygous51421949
103889651538896516TC18GENIChomozygous53139205
103889660938896610TTTTG3GENIChomozygous52876032
103889701738897018AG5GENIChomozygous51421955
103889706638897067GA15GENICpossibly homozygous53139207
103889829138898292TG16GENICpossibly homozygous51421956
103889839338898394CT16GENICpossibly homozygous53139209