chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151798617317986174TG50GENIChomozygous48241524
151798625217986253TC55GENIChomozygous48241525
151798628317986284TC50GENICpossibly homozygous48241526
151798635017986351TC47GENIChomozygous48241527
151798638917986390GGGTTT35GENIChomozygous48241528
151798640717986408TC43GENICheterozygous48241529
151798640717986408TTTTGC35GENICpossibly homozygous48241530
151798646717986468TG39GENIChomozygous48241531
151798676517986766GGA39GENIChomozygous48241532
151798721617987217AG41GENIChomozygous48241533
151798733617987337TC59GENIChomozygous48241534
151798763017987631GA50GENIChomozygous48241535