chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122418252424182525TC21GENIChomozygous50132057
122418321924183220AG14GENIChomozygous50132059
122418371924183720CT26GENICpossibly homozygous50132061
122418396924183970CT17GENIChomozygous50132063
122418402224184023AAT19GENIChomozygous50132065
122418409724184098GA33GENIChomozygous50132067
122418410324184104GC34GENIChomozygous50538432
122418410524184106CT36GENIChomozygous50538433
122418415924184160TTGCATG44GENIChomozygous50132069
122418433524184336TA39GENIChomozygous50132071
122418435924184360GGTGTGTT46GENIChomozygous50538434
122418436924184370TC49GENIChomozygous50132077
122418437524184376GT52GENIChomozygous50132079
122418438124184382GC52GENICpossibly homozygous50132081
122418447924184480GC18GENIChomozygous50538435
122418448724184488CG17GENIChomozygous50132083
122418449124184492CT16GENIChomozygous50132085
122418450124184502GGTGTC15GENIChomozygous50538436
122418453224184534TG--24GENICheterozygous50132087
122418494324184944CCTG22GENIChomozygous50132104
122418497524184976GT13GENICpossibly homozygous50132108
122418500024185001TTGC10GENICheterozygous50557683
122418517724185178CT34GENIChomozygous50132112
122418563424185635CCAAAAA5GENICheterozygous50132116
122418563424185635CCAAAA5GENICheterozygous50538437
122418563424185635CCAAAAAAAAAAAAA5GENICheterozygous50538438