chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224752546224752547TC15GENIChomozygous57111888
4224752565224752578CCGTTCCTTTCAT-------------16GENIChomozygous57111890
4224753229224753230GA53GENIChomozygous57111892
4224753689224753690CCA28GENICpossibly homozygous57111894
4224754005224754006GA59GENIChomozygous57111896
4224755022224755023CG36GENICpossibly homozygous57111897
4224755128224755129GGAA29GENICheterozygous57111899
4224755128224755129GGA29GENICpossibly homozygous57111901
4224758154224758156CG--4GENIChomozygous57111903
4224758157224758158GT29GENICheterozygous57111905
4224758589224758590TTG38GENIChomozygous57111907
4224758655224758656AG40GENIChomozygous57111909
4224758950224758951TC43GENIChomozygous57111911