chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224752546224752547TC19GENIChomozygous57111888
4224752565224752578CCGTTCCTTTCAT-------------21GENIChomozygous57111890
4224753229224753230GA25GENIChomozygous57111892
4224753689224753690CCA25GENICpossibly homozygous57111894
4224754005224754006GA21GENIChomozygous57111896
4224755022224755023CG18GENIChomozygous57111897
4224755128224755129GGA11GENIChomozygous57111901
4224758154224758156CG--13GENICheterozygous57111903
4224758589224758590TTG34GENIChomozygous57111907
4224758655224758656AG24GENIChomozygous57111909
4224758950224758951TC29GENIChomozygous57111911
4224758156224758160CGCA----17GENICheterozygous58448301