chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57052397470523975AG21GENIChomozygous113850963
57052563770525638GT16GENIChomozygous113850965
57053066570530666GA16GENIChomozygous113850969
57053091870530919GA21GENIChomozygous113850971
57053129370531294TG28GENIChomozygous113850973
57053188970531890GA11GENIChomozygous113850975
57053244670532447CT13GENIChomozygous113850977
57053290470532905GC19GENIChomozygous113850979
57053301470533015CT19GENIChomozygous113850981
57053303570533036CA22GENIChomozygous113850983
57053306370533064TC24GENIChomozygous113850985
57053312470533125GA22GENIChomozygous113850987
57053321870533219AG21GENIChomozygous113850989
57053324170533242CA20GENIChomozygous113850991
57053735370537354GC10GENIChomozygous113850993
57053806170538062AG16GENIChomozygous113850995
57054007870540079GA19GENIChomozygous113850997
57054634570546346GA21GENIChomozygous113851003
57053183370531834TC10GENIChomozygous128288985
57055459870554599CT13GENIChomozygous113851007
57056536370565364GA19GENIChomozygous113851011
57056730970567310CT20GENIChomozygous113851013
57056763770567638GA28GENIChomozygous113851015
57056813370568134AG33GENIChomozygous113851017
57056837470568375CA23GENIChomozygous113851019
57057075970570760GC19GENIChomozygous113851021
57057336970573370TC19GENIChomozygous113851023
57057435670574357GA22GENIChomozygous113851025
57057567270575673AG16GENIChomozygous113851027
57053304670533047C23GENIChomozygous128196424
57054096970540970T16GENIChomozygous128196425
57056455570564555C21GENIChomozygous128196427
57056459370564593C15GENIChomozygous128196428
57056487770564878C9GENIChomozygous128196429
57056499970565000G10GENIChomozygous128196430
57056505870565059C5GENIChomozygous128196431
57056525270565253A6GENIChomozygous128196432
57056526170565262A7GENIChomozygous128196433
57056527870565279T12GENIChomozygous128196434
57057303270573032AG18GENIChomozygous128196435