chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115004960115004961AG39GENIChomozygous112814144
4115005013115005014TC43GENIChomozygous112814146
4115006180115006181AG34GENICheterozygous112814148
4115006191115006192CT30GENICheterozygous112814150
4115006267115006268CA46GENICpossibly homozygous112814152
4115006407115006408CT54GENICheterozygous112814154
4115006419115006420TA47GENICheterozygous112814156
4115007795115007796AG57GENIChomozygous112814158
4115011173115011174TC53GENIChomozygous112814160
4115011971115011972GA33GENICpossibly homozygous112814162
4115012683115012684TC31GENICpossibly homozygous112814164
4115015886115015887AG24GENICpossibly homozygous112814166