chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14115272656115272657CT28GENIChomozygous113561429
14115273251115273252AC24GENIChomozygous113561431
14115274269115274270TC23GENIChomozygous113561433
14115274359115274360CT25GENIChomozygous113561435
14115274376115274377GA29GENIChomozygous113561437
14115274470115274471TA37GENIChomozygous113561439
14115274944115274945CT18GENIChomozygous113561441
14115275322115275323GA13GENIChomozygous113561443
14115275476115275477GA28GENIChomozygous113561445
14115274914115274915GC18GENIChomozygous113625762
14115275684115275685CA28GENICpossibly homozygous113561447
14115275714115275715AT25GENIChomozygous113561449
14115276970115276971AG21GENIChomozygous113561451
14115277219115277220AG21GENIChomozygous113561453
14115277698115277699GA21GENIChomozygous113561455
14115278384115278385TA18GENIChomozygous113561457