chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4127167512127167513GC30GENIChomozygous113383815
4127169976127169977TC27GENIChomozygous113156168
4127170114127170115CT34GENIChomozygous113156169
4127170476127170477GA25GENIChomozygous113156170
4127171310127171311GA21GENIChomozygous113156171
4127171519127171520GC16GENIChomozygous113156172
4127171671127171672AT34GENIChomozygous113156173
4127173797127173798TA19GENIChomozygous113156174
4127174498127174499GA29GENIChomozygous113156175
4127176084127176085CT24GENIChomozygous113156176
4127176232127176233CT21GENIChomozygous113156177