chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106077138960771390TC55GENICheterozygous117130854
106077139960771400AG59GENICheterozygous117996380
106077141360771414GC64GENICheterozygous117130855
106077150160771502TC77GENICheterozygous118123818
106077156060771561GA69GENIChomozygous117996386
106077163660771637GC50GENIChomozygous117219398
106077182760771828GT56GENICpossibly homozygous117196162
106077187960771880CA63GENIChomozygous117219400
106077194960771950TC42GENIChomozygous117996389
106077197860771979GT41GENIChomozygous118067639
106077204560772046AG42GENIChomozygous117996391
106077211460772115GA50GENICpossibly homozygous117996392
106077220560772206TC67GENICpossibly homozygous117996394
106077228860772289AT50GENIChomozygous116890641