chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224752546224752547TC10GENIChomozygous537640247
4224752565224752578CCGTTCCTTTCAT-------------7GENIChomozygous697190983
4224753229224753230GA41GENIChomozygous537640248
4224753689224753690CCA27GENIChomozygous697190984
4224754005224754006GA39GENIChomozygous537640249
4224755022224755023CG28GENICpossibly homozygous540935784
4224755128224755129GGAA13GENICheterozygous697190985
4224755128224755129GGA13GENICheterozygous697190986
4224758154224758156CG--10GENICheterozygous697190987
4224758157224758158GT29GENICheterozygous537640250
4224758589224758590TTG21GENIChomozygous697190988
4224758655224758656AG27GENIChomozygous537640251
4224758950224758951TC26GENIChomozygous540935785