chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
166891165468911655GGA20GENIChomozygous750841573
166891171368911714GC19GENIChomozygous639726067
166891171768911718GA18GENIChomozygous639726068
166891183068911831GA23GENIChomozygous639726069
166891195368911955GG--13GENIChomozygous750841574
166891197768911978G-14GENIChomozygous750841576
166891211068912111AAT26GENIChomozygous750841577
166891216468912166AA--23GENIChomozygous750841578
166891232668912334AGAAAAAA--------11GENICpossibly homozygous750841581
166891338668913387CT39GENIChomozygous639726070
166891370568913706CT26GENIChomozygous639726071
166891381268913813GA19GENIChomozygous639726072
166891421868914219CT21GENIChomozygous639726073
166891425268914253GGTCCTAAGGGAACTAGGCTAGGTGGGCAGGAAGCCTCTTCCACACACTTTGGCTCC24GENICheterozygous750841582
166891435068914351GA24GENIChomozygous639726074
166891441068914411AG25GENIChomozygous639726075
166891462768914628TTCTCCCTCCCTCCCTCC2GENIChomozygous750841583
166891491868914919AG18GENIChomozygous639726076
166891504268915043CCGGG14GENIChomozygous750841586
166891530668915307CCGCCGCTGCCGCCGCT11GENIChomozygous750841587