chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148059517080595171AG17GENIChomozygous144134778
148059517280595173AG17GENIChomozygous144134779
148060212280602123CT7GENICheterozygous144134798
148060811080608110A15GENIChomozygous144942333
148061197080611972AC7GENICheterozygous141096812
148060484380604844A12GENICpossibly homozygous139406685
148061304980613057CACACTCA13GENIChomozygous144942334
148062011680620116A12GENIChomozygous144107030
148063020480630208CATG8GENICpossibly homozygous144942336
148062196480621966AT14GENIChomozygous144942335
148063069080630690AACAG21GENIChomozygous144107038
148063070380630704A23GENIChomozygous144107039
148062896280628963CT13GENIChomozygous144962198
148063019180630192AG9GENICheterozygous144962199
148063019880630199CT8GENICpossibly homozygous144962200
148063020680630207TC8GENICheterozygous403363825
148063020680630207T8GENICpossibly homozygous403363824