chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187821883578218836AG43GENIChomozygous140361576
187822410978224110GA58GENICpossibly homozygous140361577
187822439178224392TC82GENIChomozygous140361578
187822497678224977GT52GENIChomozygous140361579
187822782378227824CT73GENIChomozygous140361580
187822802978228030TC41GENIChomozygous140361581
187823292378232924TG59GENICheterozygous155061067
187823442578234426GT48GENIChomozygous140361582
187823490278234903AT56GENICpossibly homozygous140361583
187823524078235241AG46GENIChomozygous140361584
187823690978236910AT12GENIChomozygous140361585
187824268178242682CT45GENIChomozygous140361586
187824312678243127CG46GENIChomozygous140361587
187824376678243767AC44GENIChomozygous140361588
187823292378232924T59GENICheterozygous403780681
187823790178237902T12GENICheterozygous149075549
187822605778226057TTTAACC58GENIChomozygous140234457