chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146062944260629443CCT11GENICheterozygous49288749
146063901060639011CT6GENIChomozygous48745076
146063901260639013CT6GENIChomozygous48745078
146063901360639014CG6GENIChomozygous48745080
146063902660639027TC12GENIChomozygous48745082
146063903160639032GA12GENIChomozygous49251745
146063903260639033AG12GENIChomozygous49251746
146063903760639038AT12GENIChomozygous48745084
146063903960639040T-14GENIChomozygous48745086
146063918060639181CCT13GENIChomozygous48745088
146063924160639242C-2GENIChomozygous48745092
146063918960639193TACA----3GENICheterozygous49424800
146065673260656733AG7GENIChomozygous48745155
146065726860657269CCT1GENIChomozygous48745161
146064806260648063C-8GENICheterozygous49161906
146065275860652759T-12GENICheterozygous49405373
146065622160656222CCAA13GENICheterozygous49339872
146065622260656223A-13GENICheterozygous49339873