chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145351836145351837TTACAC19GENICpossibly homozygous56967348
4145357637145357638GT53GENICheterozygous57512334
4145364075145364076GC41GENICheterozygous56967385
4145366004145366005GT54GENIChomozygous56967394