chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2233532604233532605CT27GENICpossibly homozygous110837540
2233532646233532647CT21GENIChomozygous110837542
2233532692233532693GA23GENICpossibly homozygous110837544
2233532727233532728TC18GENIChomozygous110837546
2233532823233532824AG27GENIChomozygous110310548
2233532848233532849GA22GENIChomozygous110310550
2233533968233533969TC19GENIChomozygous110310582
2233534621233534622CA30GENIChomozygous110837550
2233535915233535916AG31GENIChomozygous110837552
2233536802233536803TA20GENIChomozygous110310643
2233536803233536804TA20GENIChomozygous110310645
2233538373233538374AG27GENIChomozygous110310686
2233538703233538704GA26GENIChomozygous110837554
2233538791233538792TC29GENIChomozygous110310690
2233539097233539098TC15GENIChomozygous110310694
2233540258233540259GA21GENIChomozygous110837556
2233540511233540512GA35GENIChomozygous110310702
2233540760233540761TC30GENIChomozygous110310706
2233541146233541147AG24GENIChomozygous110837558
2233541793233541794GT14GENIChomozygous110310716
2233541841233541842CT17GENIChomozygous110310718
2233542053233542054TA10GENIChomozygous110310720