chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175079202550792026CT17GENIChomozygous658509242
175079206850792069GC6GENIChomozygous658509243
175079220550792206CG10GENIChomozygous658509244
175079260250792603GA26GENIChomozygous658509245
175079281050792811AG42GENIChomozygous658509246
175079289550792896AG19GENIChomozygous658509247
175079310250793103TTA7GENIChomozygous762162154
175079315150793152AC3GENIChomozygous658509248
175079318450793185AG5GENIChomozygous658509249
175079326350793264T-19GENIChomozygous762162155
175079331450793315TC17GENIChomozygous658509250
175079332850793329CT20GENIChomozygous658509251
175079337850793379CT20GENIChomozygous658509252
175079341450793415AG25GENIChomozygous658509253
175079369550793696CT18GENIChomozygous658509254
175079369650793697GA18GENIChomozygous658509255
175079393650793937AC15GENIChomozygous658509256
175079452150794522GC22GENIChomozygous658509257
175079452850794529GA23GENIChomozygous658509258
175079453750794538CT20GENIChomozygous658509259
175079455650794557GA14GENIChomozygous658509260
175079467850794679TA2GENIChomozygous658509261
175079468250794683AAT2GENIChomozygous762162156
175079505850795059GA23GENIChomozygous658509262
175079520050795201TC18GENIChomozygous658509263
175079567650795677CT51GENIChomozygous658509264
175079579050795791AT12GENIChomozygous658509265
175079672750796728GA11GENIChomozygous658509266
175079678550796786CT11GENIChomozygous658509267
175079713550797136TC19GENIChomozygous658509268
175079759550797596CT22GENIChomozygous658509269
175079842150798422TTGC38GENICpossibly homozygous762162157
175079852150798522CT35GENIChomozygous658509270
175079948750799488AC6GENIChomozygous658509271