chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124276620842766209AC22GENICpossibly homozygous66755324
124276621242766213AC19GENIChomozygous66755326
124276621642766217AC19GENIChomozygous66755328
124276622042766221AC21GENIChomozygous66755330
124276622442766225AC20GENIChomozygous66755332
124276622842766229AC17GENIChomozygous66755334
124276707942767080CA17GENIChomozygous66755338
124276804942768050AT25GENICpossibly homozygous66755340
124276845342768454TC26GENIChomozygous66755342
124277076042770761AC16GENIChomozygous66755344
124277151142771512CA11GENIChomozygous66755346