chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113390944333909444TC39GENIChomozygous116352548
113390966933909670AC67GENIChomozygous116129469
113391041933910420GA51GENIChomozygous116352549
113391242833912429GT50GENICpossibly homozygous116352550
113391345633913457GA47GENIChomozygous116352551
113391429733914298AG53GENIChomozygous116036373
113390979733909798TC52GENIChomozygous115819094
113391041633910416AGT50GENIChomozygous128897723
113391199833911999T40GENIChomozygous128897724
113391087233910873TC23GENIChomozygous131718135
113391099933910999CG20GENICheterozygous131715926
113391364033913640TTAGCCA37GENIChomozygous131715927
113391374133913787TATTTATATATATATATATATATATATATATATATATATATATATA44GENIChomozygous131715928
113391460933914610AT56GENIChomozygous115819098
113391461533914616GC58GENIChomozygous116352554
113391482133914822AG48GENICpossibly homozygous131718136
113391491733914918GA51GENICpossibly homozygous116352555
113391518833915189AG51GENIChomozygous115819100
113391678633916787GA40GENICpossibly homozygous116352556
113391727433917275TC47GENIChomozygous116352557
113391753033917531AT51GENIChomozygous116360450
113391500033915001CA51GENICpossibly homozygous116411072