chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135642534135642535T15GENICheterozygous403720353
5135642534135642535TA15GENICpossibly homozygous403720354
5135661640135661641CT2GENIChomozygous137630118
5135672488135672489GT12GENICheterozygous403159319
5135672488135672489G12GENIChomozygous403159320
5135728858135728859AT24GENIChomozygous141004720
5135792949135792950CG17GENIChomozygous137630270
5135815908135815909A17GENIChomozygous403159345
5135815908135815909AG17GENICheterozygous403159346
5135844347135844348G6GENICheterozygous403600608
5135844347135844348GA6GENICheterozygous403600609
5135844348135844349A6GENICheterozygous403600610
5135844348135844349AG6GENICheterozygous403600611
5135873253135873254TG1GENIChomozygous137630416
5135916712135916713A7GENIChomozygous403159369
5135823513135823513C18GENICheterozygous137343915
5135834910135834911T5GENIChomozygous137343924
5135834919135834919T5GENIChomozygous137343925
5135916712135916713AG7GENICheterozygous403159370
5135934909135934910TA11GENICheterozygous403159376
5135934909135934910T11GENICheterozygous403159377
5135934911135934912TA11GENICheterozygous403159378
5135934911135934912T11GENICheterozygous403159379