chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97864056778640568CCA14GENIChomozygous52026090
97865007078650071TA3GENICheterozygous52026092
97865008078650081GC1GENIChomozygous52026094
97865008578650086GA1GENIChomozygous52026096
97865008778650088CT1GENIChomozygous52026098
97865009278650093CA1GENIChomozygous52026100