chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171306324513063246GA20GENIChomozygous111295508
171306329713063298CT22GENIChomozygous111295509
171306337413063375AT16GENIChomozygous111295510
171306339913063400GC20GENIChomozygous111295511
171306382013063821AG18GENIChomozygous111295512
171306403213064033CA25GENIChomozygous119356625
171306467213064673CT22GENIChomozygous111295513
171306499913065000CT23GENIChomozygous111295514
171306520313065204AT16GENIChomozygous111295515
171306541713065418TC22GENIChomozygous111295516
171306542413065425GA21GENIChomozygous111295517
171306580813065809GC21GENIChomozygous111295518
171306581213065813GA21GENIChomozygous111295519
171306582613065827AG22GENIChomozygous111295520
171306665813066659TC33GENIChomozygous111295521
171306669713066698GA28GENIChomozygous111295522
171306727713067278TA39GENICheterozygous119265432
171306728313067284CA44GENICheterozygous119265433
171306730413067305AG57GENICheterozygous119265436
171306731113067312GA60GENICheterozygous119265437
171306731313067314CA60GENICheterozygous119265438
171306745913067460TC23GENICheterozygous119356631
171306750713067508TC20GENICheterozygous119265445
171306751913067520GA20GENICheterozygous119265446
171306787713067878AG16GENIChomozygous110962169
171306430913064310AG39GENICpossibly homozygous111612385
171306431113064312AT37GENIChomozygous111612388
171306621213066213AG20GENIChomozygous110962160
171306659913066600AG37GENIChomozygous110962163
171306681413066815AG18GENIChomozygous111295523
171306774313067744GA20GENICpossibly homozygous111295524
171306735913067360AG54GENICheterozygous119422369
171306796213067963AG21GENIChomozygous110962171
171306826813068269GA18GENIChomozygous111295525
171306837313068374TC22GENIChomozygous110962173
171306859213068593CG22GENIChomozygous110962177
171306863813068639AG26GENIChomozygous110962179