chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140564983140564984GA52GENICpossibly homozygous779958098
4140565941140565942GA57GENICheterozygous779958099
4140565949140565950GA54GENICheterozygous779958100
4140566232140566233CT27GENICheterozygous779958101
4140567416140567417TA66GENIChomozygous779958102
4140567719140567720GA52GENIChomozygous779958103
4140568687140568688CT52GENIChomozygous779958104
4140568993140568994AG60GENIChomozygous779958105
4140569239140569240AT59GENIChomozygous779958106
4140570080140570081TG48GENIChomozygous779958107
4140570084140570085AG47GENIChomozygous779958108
4140572950140572951AG49GENIChomozygous779958109
4140573002140573003AG79GENICpossibly homozygous779958110
4140573909140573910GC41GENIChomozygous779958111
4140573928140573929CT42GENIChomozygous779958112
4140574076140574077AG49GENIChomozygous779958113
4140574078140574079GA49GENIChomozygous779958114
4140574272140574273CT37GENICpossibly homozygous779958115
4140574548140574549GA70GENIChomozygous779958116
4140574608140574609CT64GENIChomozygous779958117
4140574770140574771AG61GENIChomozygous779958118
4140575255140575256GA46GENIChomozygous779958119
4140575893140575894TG50GENIChomozygous779958120
4140576235140576236TA62GENIChomozygous779958121
4140578417140578418GA61GENIChomozygous779958122
4140593585140593586CA60INTERGENIChomozygous779958123
4140593636140593637AT51INTERGENIChomozygous779958124
4140593642140593643CT47INTERGENIChomozygous779958125