chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69342369993423700TC31GENIChomozygous785477081
69342389693423897GA7GENICheterozygous785477082
69342389893423899GA6GENICheterozygous785477083
69342471193424712AG20GENIChomozygous785477084
69342516193425162AG11GENIChomozygous785477085
69342522693425227CT22GENICheterozygous785477086
69342528793425288GC15GENIChomozygous785477087
69343041293430413AG15GENIChomozygous785477088
69343203793432038GA20GENIChomozygous785477089
69343312593433126CG20GENICheterozygous785477090
69343323593433236AT27GENIChomozygous785477091
69343386593433866TA17GENIChomozygous785477092
69343643193436432TC7GENIChomozygous785477093
69343643293436433GA7GENIChomozygous785477094
69343643993436440TA7GENIChomozygous785477095
69343645493436455GA8GENIChomozygous785477096
69343650293436503CT12GENIChomozygous785477097
69343650493436505GA12GENIChomozygous785477098
69343652093436521CT15GENIChomozygous785477099
69343654393436544GT17GENIChomozygous785477100
69343654993436550CT17GENIChomozygous785477101
69343658993436590CG20GENIChomozygous785477102
69343677993436780CT25GENIChomozygous785477103
69343724293437243GT18GENIChomozygous785477104
69343753993437540GA21GENIChomozygous785477105
69344174393441744TC16GENIChomozygous785477106
69344297993442980TC23GENIChomozygous785477107