chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106077138960771390TC18GENICheterozygous117130854
106077139960771400AG19GENICheterozygous117996380
106077140260771403GA19GENICheterozygous117996382
106077141360771414GC18GENICheterozygous117130855
106077156060771561GA21GENIChomozygous117996386
106077163660771637GC24GENICpossibly homozygous117219398
106077182760771828GT27GENIChomozygous117196162
106077187960771880CA35GENIChomozygous117219400
106077194960771950TC30GENIChomozygous117996389
106077197860771979GT25GENIChomozygous118067639
106077204560772046AG18GENIChomozygous117996391
106077211460772115GA19GENICpossibly homozygous117996392
106077220560772206TC20GENICheterozygous117996394
106077228860772289AT9GENIChomozygous116890641