chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31838261118382612GC18GENIChomozygous111476195
31838262418382625TG16GENIChomozygous111476196
31838262818382629TC20GENICpossibly homozygous111476197
31838270218382703TC34GENICpossibly homozygous111476198
31838271218382713AT34GENICpossibly homozygous111476199
31838272218382723TA30GENIChomozygous111476200
31838274018382741CA20GENIChomozygous111476201
31838274118382742GA20GENIChomozygous111476202
31838281818382819CG16GENIChomozygous111476203
31838282618382827AG15GENIChomozygous111476204
31838288218382883AC9GENIChomozygous111476205
31838288718382888AT10GENIChomozygous111476206
31838288918382890CT9GENIChomozygous111476207
31838294818382949GA9GENIChomozygous111476208
31838299418382995CT10GENIChomozygous111476209
31838300518383006TA11GENIChomozygous111476210
31838302118383022TC16GENIChomozygous111476211
31838304418383045CG22GENIChomozygous111476212
31838304518383046AG22GENIChomozygous111476213
31838314218383143CA34GENIChomozygous111476214
31838316518383166CG32GENIChomozygous111476215
31838318218383183AG26GENIChomozygous111476216
31838318618383187GA25GENIChomozygous111476217