chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115451265115451266TC12GENICpossibly homozygous52826089
8115451380115451381CG10GENIChomozygous52826090
8115451567115451568AAG13GENIChomozygous52826091
8115452053115452054CT29GENIChomozygous52826092
8115452637115452638CT44GENIChomozygous52826093
8115453743115453744CCT13GENIChomozygous52826095
8115454458115454459AG22GENIChomozygous52826097
8115455591115455592CCACACACACACAT14GENIChomozygous53579901
8115457284115457285CT23GENIChomozygous52826099
8115457901115457902AG27GENIChomozygous52826100
8115458166115458167GA27GENIChomozygous52826101
8115458185115458186CT20GENIChomozygous52826102
8115458424115458425GGA16GENICpossibly homozygous52826103
8115458699115458700CCT12GENICheterozygous52826104
8115458807115458808CT17GENIChomozygous52826106
8115459272115459273T-8GENIChomozygous53305523
8115459362115459363AATTTGT20GENIChomozygous52826107
8115459782115459783TC16GENIChomozygous52826108