chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191139990911399910TC35GENIChomozygous46061568
191140414411404145CT27GENIChomozygous46061569
191140548711405488CA24GENIChomozygous46061570
191140588811405889GC24GENIChomozygous46061571
191140604611406047GA40GENIChomozygous46061572
191141699211416993AC28GENIChomozygous46061575
191141917411419175CT22GENIChomozygous46061576
191141951911419520CT37GENIChomozygous46061577
191141999311419994CT34GENIChomozygous46061578
191142018111420182GGA9GENIChomozygous46061579
191142114711421148TTAA4GENIChomozygous46061581
191142171411421715CT26GENIChomozygous46061583
191142186511421866CT10GENIChomozygous46061584
191142216411422165GGCACACA17GENICpossibly homozygous46061585
191142216611422167GA28GENIChomozygous46061586
191142244811422449TA32GENIChomozygous46061588
191142344711423448GA10GENIChomozygous46061589
191142216411422165GGCACA17GENICheterozygous46428164
191141469811414714GTGCGTGCGTGTGTGT----------------11GENICheterozygous46546906
191141470011414714GCGTGCGTGTGTGT--------------11GENICheterozygous46458891