chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2543997025439971GGCC15GENIChomozygous45110057
X2545383925453840T-11GENICpossibly homozygous45503787
X2545501525455016AG28GENIChomozygous45110070
X2545510325455107GTGT----9GENIChomozygous45877309
X2545806225458063TTAC3GENIChomozygous45566620
X2546100725461008AG14GENIChomozygous45110075
X2547783525477836A-5GENICheterozygous45110089
X2548482825484830GT--2GENIChomozygous45849304
X2548746225487464AC--2GENIChomozygous45750734
X2548870525488706GC11GENIChomozygous45867395