chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71817463718174638CT21GENIChomozygous116116255
71817643718176438GA29GENICheterozygous116116256
71817485118174852AG15GENIChomozygous116007819
71817660218176603CT25GENICheterozygous116116257
71817729118177292CA15GENIChomozygous116007822
71817779818177799TA9GENICpossibly homozygous116007823
71818013718180138TC16GENIChomozygous116116258
71818064018180641GA19GENIChomozygous116116260
71818073118180732TC19GENIChomozygous116116261
71818088318180884CT25GENIChomozygous116116262
71818099018180991AG17GENIChomozygous116116263
71818117118181172CT20GENIChomozygous116116264
71818150418181505AG20GENIChomozygous116116265
71818154118181542GT18GENIChomozygous116116266
71818182718181828GA15GENIChomozygous116116267
71818234318182344GA17GENIChomozygous116116268
71818241118182412CT22GENIChomozygous116116269
71818268318182684AG29GENIChomozygous116007826
71818278818182789AG21GENIChomozygous116116270
71818312818183129AT21GENIChomozygous116116271
71818315418183155CA20GENIChomozygous116116272
71818330818183309GA20GENIChomozygous116116273
71818333418183335GC16GENIChomozygous116116274
71818366218183663AG24GENIChomozygous116116275