chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106486638364866384AG11GENIChomozygous126384594
106486865964868660GA12GENIChomozygous126384596
106486867564868676AG5GENIChomozygous126384597
106487311564873116CT7GENIChomozygous126384599
106487321964873220CT14GENIChomozygous126384600
106487366664873667TC19GENIChomozygous126384601
106487487864874879TG9GENICheterozygous126421756
106487503864875039CT26GENIChomozygous126384602
106487915964879160TC6GENIChomozygous126384603
106487917464879175TC4GENIChomozygous126384604
106488093964880940GA14GENIChomozygous126384605
106488261364882614CT13GENIChomozygous126384606
106488273464882735AG10GENIChomozygous126384607
106488278564882786CT7GENIChomozygous126384608
106488301664883017GT12GENIChomozygous126384609
106488310264883103CG8GENIChomozygous126384610
106488373764883738CA14GENIChomozygous126384611
106488477664884777TG16GENIChomozygous126384612
106488509264885093AT17GENIChomozygous126384613
106488923164889232TC5GENIChomozygous126384616
106489028764890288CT21GENIChomozygous126384617
106490689164906892CT20GENIChomozygous126384619
106491055764910558GA18GENIChomozygous126384620
106491091464910915CG20GENIChomozygous126384621
106491125464911255AG10GENIChomozygous126384622
106491340564913406GA23GENIChomozygous126384623
106491408864914089GA17GENIChomozygous126384624
106491130764911308TG9GENICheterozygous126442164
106490035764900358CT5GENICheterozygous126442163