chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171496735414967355CT20GENIChomozygous111336387
171496913614969137TA13GENIChomozygous110966764
171497069914970700GT35GENIChomozygous111231657
171497099814970999GA44GENIChomozygous111336389
171497125814971259AG47GENIChomozygous111336391
171497157414971575CA30GENICheterozygous111336393
171497157414971575CG30GENICheterozygous111336395
171497226014972261GC24GENIChomozygous111171244
171497236814972369AG14GENIChomozygous111336397
171497343914973440CT12GENIChomozygous111336399
171497446314974464TC25GENIChomozygous111336401
171497651914976520TG31GENIChomozygous111336403
171497717214977173TA28GENIChomozygous111336405
171497674914976750AT19GENIChomozygous111171248
171497771114977712GA27GENIChomozygous111336407
171497846114978462TC23GENIChomozygous111171254
171497847414978475TC20GENIChomozygous111171256
171497855614978557GT23GENIChomozygous111171258
171497933914979340GT25GENIChomozygous111171260
171497944614979447GA33GENIChomozygous111336409
171497945514979456TC32GENIChomozygous111336411
171497946614979467AG30GENIChomozygous111336413
171497873814978739TC31GENIChomozygous111295998