chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12830297928302980CA18GENIChomozygous109067772
12831071928310720TC14GENICheterozygous120478717
12831072028310721CT14GENIChomozygous120552992
12831573928315740AG10GENIChomozygous109067774
12831869528318696TC17GENIChomozygous109067776
12831635828316359CA15GENIChomozygous108065806
12831636428316365GT10GENIChomozygous108065807
12832101228321013CT17GENIChomozygous108701278
12832588028325881TC15GENIChomozygous108701282
12833176128331762TC17GENIChomozygous108701290
12833338528333386CT16GENICheterozygous120658059
12833807928338080GA21GENIChomozygous108701293
12835073428350735AG5GENIChomozygous108701342
12836030928360310TC23GENIChomozygous108701373
12836303628363037AC12GENIChomozygous108701379
12836591428365915AG11GENIChomozygous109067784
12837044528370446AG17GENIChomozygous109067786
12837136728371368AG12GENIChomozygous108701392
12837302628373027TC22GENIChomozygous109067788
12837528228375283CT21GENIChomozygous109067790
12837700928377010CT7GENIChomozygous108701404
12837905128379052GA24GENIChomozygous109067792
12838090428380905GA8GENIChomozygous108701407
12838109528381096GA23GENIChomozygous109067794
12838169528381696TC15GENIChomozygous109067796
12838302828383029GC20GENIChomozygous109067798
12838534128385342GA21GENIChomozygous109067800
12838614728386148GA17GENIChomozygous109067802
12838794628387947CT3GENICheterozygous109067804
12839127228391273TC26GENIChomozygous108701426
12832781128327812TG4GENIChomozygous125421593