chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT38GENIChomozygous522129569
5151526224151526225AG36GENIChomozygous522129570
5151526927151526928GC37GENIChomozygous522129571
5151527610151527611T-19GENIChomozygous690731922
5151527705151527706AG5GENIChomozygous522129572
5151527853151527854CT32GENIChomozygous522129573
5151528037151528038CCT20GENICpossibly homozygous690731923
5151528037151528038CCTTTTT20GENICheterozygous690731924
5151528329151528330GA45GENIChomozygous522129574
5151529328151529329CCCAAT28GENIChomozygous690731925
5151530016151530017CA41GENIChomozygous522129575
5151530452151530453TC34GENIChomozygous522129576
5151532097151532098AAT25GENIChomozygous690731926
5151532349151532350GA44GENIChomozygous522129577
5151532466151532467AT32GENIChomozygous522129578