chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3153196447153196448GA29GENIChomozygous112187886
3153196658153196659GA33GENIChomozygous112187887
3153196799153196800GA24GENIChomozygous112187888
3153198322153198323TC39GENICheterozygous112187889
3153203333153203334GA46GENIChomozygous112187890
3153203590153203591AG39GENIChomozygous112042811
3153197603153197604GA39GENIChomozygous112366318
3153201285153201286CT28GENIChomozygous112366319
3153198254153198255CA29GENIChomozygous112042807
3153201628153201629CT43GENIChomozygous112042809
3153203692153203693AG41GENIChomozygous112042812
3153203696153203697TG37GENIChomozygous112042813
3153204084153204085GA32GENIChomozygous112187891
3153204359153204360TC36GENIChomozygous112042814
3153204453153204454AG40GENIChomozygous112042815
3153204551153204552AG42GENIChomozygous112042816
3153205353153205354CT50GENIChomozygous112042817
3153205480153205481AC39GENIChomozygous112042818
3153207032153207033AG39GENICpossibly homozygous112042820
3153207141153207142CA22GENIChomozygous112042822
3153208059153208060TC25GENIChomozygous112187892