chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64648571146485712TG41GENIChomozygous54876787
64648590746485908AT51GENIChomozygous54876788
64648611546486116TTC29GENIChomozygous54876789
64648654346486544GC41GENIChomozygous54876790
64648729846487299CT41GENIChomozygous54876791
64648740146487402CT41GENIChomozygous54876792
64648770946487710CCT47GENIChomozygous54876793
64648778746487788AG48GENIChomozygous54876794
64648785446487855G-47GENIChomozygous54876795
64648809046488091TC23GENICpossibly homozygous54876796
64648813746488138AG12GENICheterozygous54876797
64648814246488143CT15GENICpossibly homozygous54876798
64648858946488590AG41GENIChomozygous54876799
64648864946488650CG41GENIChomozygous54876800
64648870146488702TC39GENIChomozygous54876801
64648894846488949GA35GENIChomozygous54876802
64648910046489101GC32GENIChomozygous54876803
64648971946489720CT27GENIChomozygous54876804
64648975046489751CG30GENIChomozygous54876805
64648980046489801AG29GENIChomozygous54876806
64648981546489816CT31GENIChomozygous54876807
64648990546489906G-41GENIChomozygous54876808
64648992646489927CT43GENIChomozygous54876809
64648809146488093AC--5GENICheterozygous54364666