chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8114519123114519124CT8GENICpossibly homozygous53982527
8114519189114519190CG1GENIChomozygous52824021
8114521493114521494CG16GENICpossibly homozygous52824023
8114523082114523083GA8GENIChomozygous53982529
8114523316114523317GA15GENIChomozygous52824026
8114523679114523680CA16GENICpossibly homozygous53982531
8114523767114523768TG12GENICpossibly homozygous53982533
8114526763114526764TG5GENIChomozygous52824030
8114528238114528239AG3GENIChomozygous52824031
8114528829114528830CCTTTTTTT1GENIChomozygous52824032
8114529535114529536C-16GENICheterozygous52824044