chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
23063584330635844CT22GENIChomozygous120187914
23063623530636236GA30GENIChomozygous120187915
23063636130636362GT27GENIChomozygous109675312
23063708230637083AT31GENIChomozygous109675314
23063827730638278AT31GENIChomozygous120187916
23063991530639916AG31GENIChomozygous120187917
23064018530640186CT41GENIChomozygous120187918
23064272030642721GA15GENIChomozygous120187919
23064293230642933CT45GENIChomozygous120187920
23064406830644069TC4GENIChomozygous120165449
23064458230644583GT33GENIChomozygous120187921
23064533830645339TG36GENIChomozygous109675326
23064654230646543TC45GENIChomozygous120187922
23064671030646711CT33GENIChomozygous109675328
23064736130647362CT45GENIChomozygous120187923
23064803230648033GA24GENIChomozygous120187924
23064849730648498AC21GENIChomozygous120187925
23065035930650360GA27GENIChomozygous109675334
23065349230653493CT25GENIChomozygous120187926
23065350530653506TA17GENIChomozygous120187927
23065672930656730GA33GENIChomozygous120187928
23065787830657879TG40GENIChomozygous109675338
23065840130658402AG31GENIChomozygous109675340
23065913730659138TG22GENIChomozygous120187929
23066002530660026AG32GENIChomozygous120165478
23066072730660728AC23GENIChomozygous109675346
23066326130663262TG25GENIChomozygous120187930
23066424730664248GA22GENIChomozygous109675348