chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157745073157745074TC13GENICheterozygous114070412
5157745450157745451CT3GENICheterozygous114452449
5157745477157745478AG4GENIChomozygous114070413
5157745479157745480TC4GENIChomozygous114070414
5157745829157745830GC35GENIChomozygous114070415
5157746257157746258CT35GENIChomozygous114070416
5157746304157746305AG40GENIChomozygous114070417
5157746872157746873TG25GENICpossibly homozygous114070418
5157746896157746897TC25GENIChomozygous114070419
5157746973157746974AG30GENIChomozygous114070420
5157747175157747176AG33GENIChomozygous114070421
5157747707157747708CT40GENIChomozygous114070422
5157749025157749026TC35GENIChomozygous114070423
5157749406157749407CT31GENIChomozygous114070424
5157749466157749467TC29GENIChomozygous114070425
5157750347157750348TC24GENIChomozygous114070426
5157750759157750760CT21GENIChomozygous114070427
5157751672157751673CT41GENICpossibly homozygous114070428
5157751856157751857AG45GENIChomozygous114070429
5157751868157751869GA44GENIChomozygous114070430
5157751929157751930TC41GENIChomozygous114070431
5157752577157752578CG39GENIChomozygous114070432
5157753156157753157GA27GENIChomozygous114070433
5157753334157753335AG33GENIChomozygous114070434
5157754404157754405AG25GENIChomozygous114070435
5157755525157755526GA37GENIChomozygous114070436
5157756701157756702AG23GENIChomozygous114070437
5157757567157757568CA25GENIChomozygous114070438
5157758077157758078CT33GENIChomozygous114070439
5157759201157759202AG39GENIChomozygous114070440
5157759249157759250AC35GENIChomozygous114070441