chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157745829157745830GC41GENIChomozygous114070415
5157746257157746258CT32GENIChomozygous114070416
5157746304157746305AG32GENIChomozygous114070417
5157746872157746873TG30GENIChomozygous114070418
5157746896157746897TC30GENIChomozygous114070419
5157746973157746974AG38GENIChomozygous114070420
5157747175157747176AG40GENIChomozygous114070421
5157747707157747708CT28GENIChomozygous114070422
5157747748157747749AG17GENIChomozygous114651903
5157747749157747750TA17GENIChomozygous118847126
5157749025157749026TC24GENIChomozygous114070423
5157749406157749407CT40GENIChomozygous114070424
5157749466157749467TC35GENIChomozygous114070425
5157750759157750760CT35GENIChomozygous114070427
5157751672157751673CT44GENIChomozygous114070428
5157751856157751857AG32GENIChomozygous114070429
5157751868157751869GA31GENIChomozygous114070430
5157751929157751930TC28GENIChomozygous114070431
5157752577157752578CG23GENIChomozygous114070432
5157753156157753157GA24GENIChomozygous114070433
5157753334157753335AG16GENIChomozygous114070434
5157754287157754288CT4GENIChomozygous119085561
5157754404157754405AG12GENIChomozygous114070435
5157755525157755526GA13GENIChomozygous114070436
5157756701157756702AG24GENIChomozygous114070437
5157757567157757568CA28GENIChomozygous114070438
5157758077157758078CT34GENIChomozygous114070439
5157759201157759202AG25GENIChomozygous114070440
5157759249157759250AC28GENIChomozygous114070441