chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103703231137032312GA10GENIChomozygous126418087
103703236637032367TC15GENIChomozygous126418089
103703447237034473TA22GENIChomozygous126418091
103703492037034921GA27GENIChomozygous126418093
103703744537037446CT14GENIChomozygous126418095
103703943437039435CT17GENIChomozygous126418097
103704237537042376GC24GENICpossibly homozygous126418099
103704304037043041CT16GENIChomozygous126418101
103704623837046239CT24GENIChomozygous126418103
103704656237046563TC7GENIChomozygous126418105
103704673137046732TC13GENIChomozygous126418107
103704732237047323TC23GENIChomozygous126418109
103704774137047742GC11GENIChomozygous126418111
103704817037048171TA17GENIChomozygous126380602