chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115438052454380525CG25GENIChomozygous115869199
115438120954381210GA30GENIChomozygous115869201
115438236954382370AG13GENIChomozygous115869203
115438268854382689AT20GENIChomozygous115869205
115438364554383646TC11GENIChomozygous115869207
115438419954384200TA18GENIChomozygous115968328
115438427854384279AG28GENIChomozygous115869209
115438491654384917GT23GENIChomozygous115869211
115438640854386409AG26GENIChomozygous115869213
115438693754386938AG30GENIChomozygous115869215
115438700354387004TC31GENIChomozygous115869217
115438730454387305CG21GENIChomozygous115869219
115438731254387313CT21GENIChomozygous115869221
115438753354387534GA23GENIChomozygous115869223
115438918954389190AG17GENIChomozygous115869225
115439060654390607CT17GENIChomozygous115869227
115439513854395139AG30GENIChomozygous115869229
115439514754395148CT26GENIChomozygous115869231
115439901454399015TC32GENIChomozygous115869233
115439940954399410CT23GENIChomozygous115869235
115440303754403038TC38GENICpossibly homozygous115869237
115440315454403155AG41GENIChomozygous115869239
115440443054404431CA22GENIChomozygous115869241
115440453454404535TC18GENIChomozygous115869243