chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4118551002118551003TC21GENIChomozygous112822377
4118552139118552140CT45GENIChomozygous112822379
4118567733118567734CT53GENICheterozygous112822381
4118567756118567757TA66GENICpossibly homozygous112822383
4118570999118571000TC39GENICpossibly homozygous112822385
4118571001118571002AT40GENICpossibly homozygous112822387
4118574331118574332CT41GENIChomozygous112822389
4118579141118579142AG43GENIChomozygous112822391
4118583390118583391GT49GENICpossibly homozygous112822393