chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122418252424182525TC8GENIChomozygous50132057
122418321924183220AG15GENIChomozygous50132059
122418371924183720CT15GENIChomozygous50132061
122418396924183970CT15GENIChomozygous50132063
122418402224184023AAT16GENIChomozygous50132065
122418409724184098GA17GENIChomozygous50132067
122418410324184104GC16GENIChomozygous50538432
122418410524184106CT15GENIChomozygous50538433
122418415924184160TTGCATG27GENIChomozygous50132069
122418433524184336TA23GENIChomozygous50132071
122418435924184360GGTGTGTT22GENIChomozygous50538434
122418436924184370TC17GENIChomozygous50132077
122418437524184376GT17GENIChomozygous50132079
122418438124184382GC20GENIChomozygous50132081
122418447924184480GC10GENIChomozygous50538435
122418448724184488CG8GENIChomozygous50132083
122418449124184492CT8GENIChomozygous50132085
122418450124184502GGTGTC9GENIChomozygous50538436
122418453224184534TG--12GENICheterozygous50132087
122418494324184944CCTG15GENIChomozygous50132104
122418498724184988CCTGTG2GENIChomozygous50561447
122418563424185635CCAAAAAAAAAAAAA9GENIChomozygous50538438
122418497324184974GGTTTGTGTGTGTGTC9GENIChomozygous50607903