chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115451265115451266TC30GENIChomozygous52826089
8115451380115451381CG25GENIChomozygous52826090
8115451567115451568AAG23GENIChomozygous52826091
8115452053115452054CT35GENICpossibly homozygous52826092
8115452637115452638CT65GENIChomozygous52826093
8115453743115453744CCT35GENICpossibly homozygous52826095
8115454458115454459AG35GENIChomozygous52826097
8115455591115455592CCACACACACACAT24GENIChomozygous53579901
8115457284115457285CT40GENIChomozygous52826099
8115457901115457902AG44GENIChomozygous52826100
8115458166115458167GA45GENIChomozygous52826101
8115458185115458186CT41GENIChomozygous52826102
8115458424115458425GGA39GENICpossibly homozygous52826103
8115458699115458700CCT30GENICpossibly homozygous52826104
8115458807115458808CT36GENIChomozygous52826106
8115459272115459273T-32GENIChomozygous53305523
8115459362115459363AATTTGT30GENIChomozygous52826107
8115459782115459783TC34GENIChomozygous52826108