chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2211532781211532782AG42GENIChomozygous136459195
2211533184211533185TC34GENIChomozygous136459196
2211534400211534401TC44GENIChomozygous136459197
2211534721211534722GA38GENIChomozygous136459198
2211536156211536157GC32GENIChomozygous136459199
2211537794211537795TC43GENIChomozygous136459200
2211539676211539677GA36GENIChomozygous136459201
2211540728211540728CACT34GENIChomozygous135977224
2211543260211543260T42GENICpossibly homozygous135977225
2211545723211545724TG59GENIChomozygous136459202
2211546538211546539AG15GENICpossibly homozygous136459203