chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85083205550832056AC27GENIChomozygous53116306
85083206850832069GC26GENIChomozygous53116307
85083241050832411AC22GENIChomozygous53116308
85083245850832459CA27GENIChomozygous53116309
85083253350832534TC30GENIChomozygous53116310
85083281350832814GA10GENIChomozygous53116311
85083283050832831GT10GENIChomozygous53116312
85083303150833033AT--2GENIChomozygous53610902
85083308150833082CT3GENICheterozygous53507340
85083312450833125AAGG6GENICheterozygous53430558
85083322450833225TC14GENIChomozygous53116317
85083342850833429TA13GENIChomozygous53116318
85083344350833444TC17GENIChomozygous53116319
85083493250834933GA27GENIChomozygous53116320
85083495550834956AG20GENIChomozygous53116321
85083565650835657AG28GENIChomozygous53116322
85083628150836282CT35GENIChomozygous53116323
85083670550836706AC24GENIChomozygous53116324
85083683250836840ACACACAC--------9GENICheterozygous53430560
85083683650836840ACAC----9GENICpossibly homozygous53430562
85083687550836876CG21GENIChomozygous53430564
85083728150837283CA--18GENIChomozygous53386121
85083728350837284GGTC19GENIChomozygous53386122
85083728650837287T-20GENIChomozygous53116327
85083740250837403GA35GENIChomozygous53116328
85083762150837622TC32GENIChomozygous53116329
85083777250837773AG29GENIChomozygous53116330
85083793750837938CT29GENIChomozygous53116331
85083838650838387TC24GENIChomozygous53116332
85083841050838412GC--19GENIChomozygous53116333
85083849250838493CT21GENIChomozygous53116335
85083879850838799GGTC17GENICpossibly homozygous53116336
85083938350839384GA32GENIChomozygous53116337
85083944450839445TC17GENIChomozygous53116338