chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT22GENIChomozygous561029644
5151526224151526225AG25GENIChomozygous561029645
5151526927151526928GC26GENIChomozygous561029646
5151527610151527611T-9GENIChomozygous707117805
5151527853151527854CT26GENIChomozygous561029647
5151528037151528038CCT13GENIChomozygous707117807
5151528329151528330GA40GENIChomozygous561029648
5151529328151529329CCCAAT16GENIChomozygous707117811
5151530016151530017CA26GENIChomozygous561029649
5151530452151530453TC29GENIChomozygous561029650
5151532097151532098AAT14GENIChomozygous707117813
5151532349151532350GA21GENIChomozygous561029651
5151532466151532467AT16GENIChomozygous561029652