chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101410592514105926TC22GENIChomozygous51810147
101410600514106006CA24GENIChomozygous51622751
101410644014106441TC22GENIChomozygous51810149
101410647714106478GC16GENIChomozygous51810151
101410685014106854TGTA----18GENIChomozygous51810153
101410761614107617AG22GENIChomozygous51810155
101410839214108393GGA26GENIChomozygous51810157
101410894214108943CCA11GENICheterozygous51810159
101410894414108948AAAC----15GENICpossibly homozygous51622753
101410894714108948CCA9GENICpossibly homozygous51622754
101410903814109039AG30GENIChomozygous51810163
101410927114109272CA25GENIChomozygous51810165
101410928214109283TA24GENIChomozygous51810167
101410964914109650CCA7GENICpossibly homozygous51622755
101410975114109752A-12GENIChomozygous51622756
101410989914109900GT25GENIChomozygous51622757
101411130414111305GA18GENIChomozygous51810170
101411135514111356GA25GENIChomozygous51810172