chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230273067230273068TC31GENIChomozygous59431553
2230273076230273077CT30GENIChomozygous59431554
2230273154230273155TC23GENIChomozygous59431555
2230273575230273576GA22GENIChomozygous59431556
2230273788230273789TC27GENIChomozygous59431557
2230274399230274400GA42GENIChomozygous59431558
2230274470230274471GT28GENIChomozygous59431559
2230275541230275542AG24GENIChomozygous59431560
2230277516230277517TC29GENIChomozygous59431561
2230277985230277986TC11GENICpossibly homozygous59431562
2230278182230278183TC26GENIChomozygous59431563
2230278184230278185A-26GENIChomozygous59431564
2230278259230278260GA17GENIChomozygous59431565