chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57052397470523975AG30GENIChomozygous113850963
57052563770525638GT20GENIChomozygous113850965
57053066570530666GA29GENIChomozygous113850969
57053091870530919GA26GENIChomozygous113850971
57053129370531294TG31GENIChomozygous113850973
57053188970531890GA13GENIChomozygous113850975
57053244670532447CT28GENIChomozygous113850977
57053290470532905GC21GENIChomozygous113850979
57053301470533015CT37GENIChomozygous113850981
57053306370533064TC31GENIChomozygous113850985
57053312470533125GA24GENIChomozygous113850987
57053321870533219AG30GENIChomozygous113850989
57053324170533242CA29GENIChomozygous113850991
57054634570546346GA20GENIChomozygous113851003
57055459870554599CT26GENIChomozygous113851007
57056730970567310CT23GENIChomozygous113851013
57056763770567638GA27GENIChomozygous113851015
57056813370568134AG18GENIChomozygous113851017
57056837470568375CA18GENIChomozygous113851019
57057075970570760GC24GENIChomozygous113851021
57057336970573370TC31GENIChomozygous113851023
57057435670574357GA27GENIChomozygous113851025
57057567270575673AG36GENIChomozygous113851027
57055410570554106TA29GENICheterozygous119063741