chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98227481482274815CT18GENIChomozygous53641231
98227614282276143AAT1GENIChomozygous53641232
98227728182277282CT18GENICpossibly homozygous53641233
98227739782277398GC13GENIChomozygous52269263
98227796382277964CT19GENIChomozygous53641234
98227861882278619GGGACCAGACTAATGCC4GENICheterozygous52269267
98228061482280615CA12GENICpossibly homozygous53641235
98228094682280947AAAAAACAAAAC4GENIChomozygous53641236