chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8128779767128779775CCCTTGCC18GENIChomozygous131055758
8128779808128779809GA16GENIChomozygous116722030
8128780153128780154AC13GENIChomozygous116722031
8128780206128780207TC16GENIChomozygous116722032
8128780251128780252AG17GENIChomozygous116722033
8128780343128780343T17GENICpossibly homozygous131055759
8128780777128780778CG19GENIChomozygous116722034
8128780392128780404GAATGAATGAAT13GENIChomozygous128647241
8128779858128779859GA16GENIChomozygous117072979
8128781049128781050G20GENIChomozygous131055760
8128781051128781054CAG20GENIChomozygous131055761
8128781387128781388CT18GENIChomozygous117072981
8128781389128781390GA18GENIChomozygous116722035
8128781430128781431TC20GENIChomozygous116722036
8128781487128781488TC19GENIChomozygous116722037
8128781643128781644CT15GENIChomozygous116722038