chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1726123932612394AG22GENIChomozygous111516964
1726149082614909TC27GENICpossibly homozygous111516966
1726168072616808GA17GENIChomozygous111516968
1726180872618088CT14GENIChomozygous111516970
1726267932626794CT28GENIChomozygous111516973
1726289772628978GA38GENIChomozygous111516975
1726302622630263AG24GENIChomozygous111516977
1726319552631956TC6GENIChomozygous111380065
1726325972632598CT13GENIChomozygous111516979
1726445882644589AC45GENICpossibly homozygous111380071
1726484712648472CT27GENIChomozygous111516981
1726486922648693TA9GENICheterozygous111380073
1726457772645778CA13GENIChomozygous110937222
1726463192646320CT32GENIChomozygous111556000
1726456192645620CA6GENIChomozygous111152767
1726456432645644AC4GENIChomozygous111152769
1726515182651519AT54GENIChomozygous111516983
1726521742652175TC38GENIChomozygous111380078
1726562462656247AC7GENIChomozygous110937225
1726606012660602TC25GENIChomozygous111556003
1726600222660023CT35GENIChomozygous111516985