chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8114519189114519190CG14GENIChomozygous52824021
8114519966114519967TTGG1GENIChomozygous53047765
8114520916114520917GA11GENICpossibly homozygous52824022
8114521493114521494CG21GENIChomozygous52824023
8114521700114521701TA14GENICpossibly homozygous52824024
8114522744114522745GT15GENICheterozygous52824025
8114523316114523317GA24GENIChomozygous52824026
8114526763114526764TG10GENICpossibly homozygous52824030
8114528238114528239AG7GENIChomozygous52824031
8114529535114529536C-35GENICheterozygous52824044