chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122418252424182525TC23GENIChomozygous50132057
122418321924183220AG17GENIChomozygous50132059
122418371924183720CT17GENIChomozygous50132061
122418396924183970CT24GENIChomozygous50132063
122418402224184023AAT24GENIChomozygous50132065
122418409724184098GA22GENIChomozygous50132067
122418410324184104GC21GENIChomozygous50538432
122418410524184106CT21GENIChomozygous50538433
122418415924184160TTGCATG19GENIChomozygous50132069
122418433524184336TA29GENIChomozygous50132071
122418435924184360GGTGTGTT38GENIChomozygous50538434
122418436924184370TC35GENIChomozygous50132077
122418437524184376GT37GENIChomozygous50132079
122418438124184382GC40GENIChomozygous50132081
122418447924184480GC17GENIChomozygous50538435
122418448724184488CG13GENIChomozygous50132083
122418449124184492CT15GENIChomozygous50132085
122418450124184502GGTGTC19GENIChomozygous50538436
122418453224184534TG--19GENICpossibly homozygous50132087
122418494324184944CCTG29GENIChomozygous50132104
122418497524184976GT18GENIChomozygous50132108
122418517724185178CT33GENIChomozygous50132112
122418563424185635CCAAAAA5GENICheterozygous50132116
122418563424185635CCAAAAAAAAAAAAA5GENICheterozygous50538438
122418498724184988CCTGTG8GENIChomozygous50561447