chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115451265115451266TC15GENIChomozygous52826089
8115451380115451381CG10GENIChomozygous52826090
8115451567115451568AAG13GENIChomozygous52826091
8115452053115452054CT27GENIChomozygous52826092
8115452637115452638CT29GENIChomozygous52826093
8115453743115453744CCT12GENICpossibly homozygous52826095
8115454458115454459AG21GENIChomozygous52826097
8115455591115455592CCACACACACACAT11GENICpossibly homozygous53579901
8115457284115457285CT22GENIChomozygous52826099
8115457901115457902AG21GENIChomozygous52826100
8115458166115458167GA21GENIChomozygous52826101
8115458185115458186CT25GENIChomozygous52826102
8115458424115458425GGA18GENIChomozygous52826103
8115458699115458700CCT29GENICheterozygous52826104
8115458807115458808CT18GENIChomozygous52826106
8115459272115459273T-20GENICpossibly homozygous53305523
8115459362115459363AATTTGT25GENIChomozygous52826107
8115459782115459783TC29GENIChomozygous52826108