chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5168126610168126611CA39GENIChomozygous794076361
5168127027168127028CT55GENIChomozygous794076362
5168128029168128030TC71GENIChomozygous794076363
5168128178168128179CT43GENICpossibly homozygous794076364
5168130962168130963GA35GENIChomozygous794076365
5168131103168131104CT66GENIChomozygous794076366
5168131868168131869CT39GENIChomozygous794076367
5168132020168132021CT44GENIChomozygous794076368
5168132288168132289AG39GENIChomozygous794076369
5168136058168136059GA38GENIChomozygous794076370