chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115451265115451266TC11GENIChomozygous52826089
8115451380115451381CG14GENIChomozygous52826090
8115451567115451568AAG15GENIChomozygous52826091
8115452053115452054CT32GENICpossibly homozygous52826092
8115452637115452638CT28GENIChomozygous52826093
8115453743115453744CCT16GENICheterozygous52826095
8115454458115454459AG18GENIChomozygous52826097
8115455591115455592CCACACACACACAT9GENIChomozygous53579901
8115457284115457285CT33GENIChomozygous52826099
8115457901115457902AG31GENIChomozygous52826100
8115458166115458167GA33GENIChomozygous52826101
8115458185115458186CT31GENIChomozygous52826102
8115458424115458425GGA18GENICpossibly homozygous52826103
8115458699115458700CCT11GENICpossibly homozygous52826104
8115458807115458808CT18GENIChomozygous52826106
8115459272115459273T-15GENIChomozygous53305523
8115459362115459363AATTTGT17GENICpossibly homozygous52826107
8115459782115459783TC28GENIChomozygous52826108