chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181793716117937162AG56GENIChomozygous782878319
181793720017937201AG53GENIChomozygous782878320
181793727217937273CT71GENICpossibly homozygous782878321
181793737717937378CG71GENIChomozygous782878322
181793755417937555AC45GENIChomozygous782878323
181793780617937807GA53GENIChomozygous782878324
181793805517938056AG48GENIChomozygous782878325
181793814417938145AG40GENIChomozygous782878326
181793815417938155CT49GENIChomozygous782878327