chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185675654556756546AC12GENICheterozygous185782538
185675654856756549AC12GENICheterozygous185782539
185675671556756716TC22GENIChomozygous185782540
185675678956756790CG16GENIChomozygous185782541
185675687656756877CA14GENICpossibly homozygous185782542
185675745456757455CG10GENIChomozygous185782543
185675746356757464AG11GENIChomozygous185782544
185675749656757497AC10GENIChomozygous185782545
185675826256758263TA28GENIChomozygous185782546
185675837656758377AT19GENIChomozygous185782547
185675881056758811GA21GENIChomozygous185782548
185675882756758828CG3GENIChomozygous185782549
185675888056758881CT16GENIChomozygous185782550
185675896656758967CT15GENIChomozygous185782551
185675911956759120GA17GENIChomozygous185782552
185676041056760411CT4GENIChomozygous185782553
185676103456761035TC24GENIChomozygous185782554
185676215356762154CA17GENIChomozygous185782555
185676358956763590TC14GENIChomozygous185782556