chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181521266215212662G25GENIChomozygous129517743
181521271415212715CG19GENIChomozygous110644270
181521273915212740C18GENIChomozygous129517744
181521275215212753T21GENIChomozygous129517745
181521275515212756A20GENIChomozygous129517746
181521281015212811C20GENIChomozygous129517747
181521290315212903G3GENIChomozygous130471463
181521303515213035G3GENIChomozygous129517748
181521310115213102C25GENIChomozygous129517749
181521317815213179G24GENIChomozygous129517750
181521322615213227G11GENIChomozygous129517751
181521725415217255G9GENIChomozygous129517755
181521762915217630T23GENIChomozygous129517756
181521767115217672C19GENIChomozygous129517757
181521769115217692G14GENIChomozygous129517758
181521780515217806T2GENIChomozygous129517761
181521775615217756G8GENIChomozygous129517759
181521778715217788A3GENIChomozygous129517760