chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10101168904101168905CA51GENIChomozygous51580645
10101168925101168926CA49GENIChomozygous51580647
10101170306101170307G-28GENIChomozygous51580651
10101170617101170618CT52GENIChomozygous51580653
10101170719101170720AG61GENIChomozygous51580655
10101170940101170941TC47GENIChomozygous51580657
10101171866101171876ACACACACAC----------5GENICheterozygous51580659
10101172113101172114CA54GENIChomozygous51580661
10101172114101172115TA52GENIChomozygous51580663
10101173083101173084GT66GENIChomozygous51580665
10101174152101174153TC52GENIChomozygous51580667
10101175299101175300CT61GENIChomozygous51580669