chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155314998155314999AC36GENICheterozygous113246799
4155320765155320766AG39GENIChomozygous112895316
4155322208155322209AT48GENICpossibly homozygous112895318
4155324176155324177CA45GENICpossibly homozygous112895320
4155328588155328589TC40GENIChomozygous112895322
4155329005155329006CG12GENICheterozygous113307908
4155329007155329008CG13GENICheterozygous112895324
4155332652155332653CT39GENIChomozygous112895326
4155332759155332760TC47GENIChomozygous112895328
4155334523155334524TG25GENIChomozygous112895330
4155334851155334852TG2GENIChomozygous112895332