chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3100991369100991370TTC5GENIChomozygous57578739
3101000762101000763TTC9GENIChomozygous57578743
3101029663101029664TTA2GENICheterozygous57933307
3101031904101031905CT10GENIChomozygous57578753
3101031905101031906CT10GENIChomozygous57578755
3101031907101031908CA10GENIChomozygous57578757
3101039074101039075CCTTA3GENIChomozygous57578763
3101039295101039296GT5GENIChomozygous57578765
3101039298101039299GA4GENIChomozygous57578767
3101039301101039302TA4GENIChomozygous57933331
3101039302101039303TC4GENIChomozygous57578769
3101039304101039305AC4GENIChomozygous57578771
3101039308101039309TC1GENIChomozygous57578773
3101039312101039313TC1GENIChomozygous57578775
3101039319101039320TC2GENIChomozygous57578777
3101039335101039336TG7GENICpossibly homozygous57578779
3101051381101051382C-2GENIChomozygous57578797
3101051387101051388C-3GENICheterozygous57578801
3101053740101053741AAAC2GENICheterozygous58650602