chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48284067682840676GAGGG26GENICpossibly homozygous128054884
48284070382840704G26GENIChomozygous128054885
48284076982840769A20GENIChomozygous128054886
48284078082840781T19GENIChomozygous128054887
48284078582840785C19GENIChomozygous128054888
48290533382905334C16GENIChomozygous128054911
48297026582970266AT16GENIChomozygous112751933
48297026982970270AC15GENIChomozygous112751935
48297027182970272AC16GENIChomozygous112751937
48297242982972430T31GENICheterozygous130296614
48299618682996196ATCCATCCTT10GENIChomozygous129902877
48299628882996289GC4GENICheterozygous113461875
48303882483038824C12GENIChomozygous128054936
48304585783045859CA21GENIChomozygous128054939
48304586283045863C21GENIChomozygous128054940