chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101168904101168905CA11GENIChomozygous51580645
10101168925101168926CA12GENICpossibly homozygous51580647
10101170306101170307G-1GENIChomozygous51580651
10101170617101170618CT19GENICheterozygous51580653
10101170719101170720AG20GENIChomozygous51580655
10101170940101170941TC25GENIChomozygous51580657
10101172113101172114CA3GENIChomozygous51580661
10101172114101172115TA3GENIChomozygous51580663
10101173083101173084GT21GENIChomozygous51580665
10101174152101174153TC24GENIChomozygous51580667
10101175299101175300CT9GENICheterozygous51580669