chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
712143301214331AT16GENIChomozygous115533133
712145761214577CG16GENIChomozygous116112473
712145791214580CA18GENIChomozygous115533134
712149081214909AG13GENIChomozygous115533135
712149131214914AT12GENIChomozygous115533136
712149661214967GT18GENIChomozygous115533138
712157881215789TG34GENIChomozygous115533139
712158351215836CA29GENIChomozygous115533140
712527621252763CA8GENIChomozygous115973323
712626431262644GC19GENICpossibly homozygous115533167
712844381284439CG5GENIChomozygous115533173