chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166479928364799284CT37GENIChomozygous111846579
166479943864799439AC35GENIChomozygous112069244
166479954164799542TC60GENIChomozygous112173584
166480031664800317AG53GENIChomozygous112069246
166480062064800621AG55GENICpossibly homozygous112173586
166479992364799924GA48GENICpossibly homozygous119221046
166480036064800361CT53GENIChomozygous112069248
166480175564801756TC43GENIChomozygous111846580
166480190264801903GT37GENIChomozygous111846581
166480225864802259GA36GENIChomozygous111846582
166480241364802414TC41GENIChomozygous111846583
166480251364802514AG40GENIChomozygous111846584
166480263264802633CA23GENIChomozygous112252401
166480297064802971CT36GENIChomozygous112069250
166480313564803136CA54GENIChomozygous112069252
166480327664803277GT39GENIChomozygous111846587
166480335664803357CT44GENIChomozygous111846588
166480341364803414AC53GENICpossibly homozygous112015762
166480487964804880TC35GENIChomozygous111846590