chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2069043546904355TTG2GENICheterozygous45676202
2069056316905635AGAG----22GENIChomozygous45972971
2069070116907012AAAG18GENIChomozygous45406243
2069095126909513A-7GENICheterozygous45735701
2069095316909535AAAA----12GENICheterozygous45879042
2069095466909549AAG---15GENICheterozygous45840639
2069095496909550A-11GENICheterozygous45972972
2069100116910012GA11GENICpossibly homozygous45406287
2069111216911127GTGTGT------3GENICheterozygous46012952
2069111256911127GT--3GENICheterozygous45840640
2069150796915080TC23GENIChomozygous45406323
2069150956915097CT--15GENIChomozygous45972973
2069167696916770TC19GENIChomozygous45406332
2069169736916974TTACACACACACACAC2GENIChomozygous45972974
2069173086917309CT17GENIChomozygous45972975
2069178056917806AG30GENIChomozygous45972976