chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182738801727388018T19GENICpossibly homozygous140216975
182739834227398343C10GENICheterozygous147618436
182739834327398344T9GENICheterozygous403431380
182739834327398344TA9GENICheterozygous403431381
182740432927404330G11GENICpossibly homozygous403431382
182740432927404330GT11GENICheterozygous403431383
182740141527401416CG18GENICheterozygous145222766
182740141627401417CT18GENICheterozygous145222767
182740141727401418AG18GENICheterozygous145222768