chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
26389616563896166CG45GENIChomozygous58850031
26389761663897617CT16GENICpossibly homozygous59701667
26389763363897634GC13GENICpossibly homozygous59701669
26389763963897643CCCT----7GENICheterozygous58850033
26389766263897663CT6GENICheterozygous58850035
26389851463898515CCTCCT54GENIChomozygous59701671
26389852663898527TA60GENIChomozygous59701673
26389871463898715CT62GENIChomozygous59701675
26389880263898803AG66GENIChomozygous59701677