chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52414424924144250TC17GENIChomozygous56206182
52414635924146360CT20GENICpossibly homozygous56206183
52414729524147296CG12GENICheterozygous56206184
52414772424147725CG21GENIChomozygous56206185
52414811124148112TC8GENIChomozygous56206186
52414956924149570TC23GENIChomozygous56206188
52414959724149598AG24GENIChomozygous56206189
52415085424150855CT12GENIChomozygous56206190
52415195124151952GGT4GENICheterozygous56206192
52415202324152024T-1GENIChomozygous56206193
52415281824152819TC21GENIChomozygous56206194
52415314824153149TC9GENICheterozygous56206196