chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5121829683121829684CT63GENICpossibly homozygous137606327
5121829975121829976T64GENIChomozygous137337715
5121832235121832236GT67GENIChomozygous137606329
5121836649121836650AG60GENIChomozygous137606332
5121832390121832405CCTCCCCCTGCAGAT71GENIChomozygous144701251
5121837965121837966TC81GENIChomozygous137606333
5121839054121839055AT63GENICpossibly homozygous137606334
5121840530121840531TC65GENIChomozygous137606335
5121844182121844185AAA54GENIChomozygous137337717
5121844188121844191AAA55GENIChomozygous137337718
5121831405121831406GA64GENIChomozygous144739914