chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT12GENIChomozygous577511598
5151526224151526225AG18GENIChomozygous577511599
5151526927151526928GC12GENIChomozygous577511600
5151527610151527611T-13GENIChomozygous716383132
5151527853151527854CT11GENIChomozygous577511601
5151528037151528038CCT9GENICheterozygous716383134
5151528037151528038CCTT9GENICheterozygous716383135
5151528329151528330GA27GENIChomozygous577511602
5151529328151529329CCCAAT18GENIChomozygous716383138
5151530016151530017CA26GENIChomozygous577511603
5151530452151530453TC21GENIChomozygous577511604
5151532097151532098AAT13GENIChomozygous716383140
5151532349151532350GA9GENIChomozygous577511605
5151532466151532467AT18GENIChomozygous577511606