chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT17GENIChomozygous567721916
5151526224151526225AG14GENIChomozygous567721917
5151526927151526928GC20GENIChomozygous567721918
5151527610151527611T-6GENIChomozygous710120794
5151527853151527854CT9GENIChomozygous567721919
5151528037151528038CCT7GENICpossibly homozygous710120796
5151528037151528038CCTT7GENICheterozygous710120797
5151528329151528330GA18GENIChomozygous567721920
5151529328151529329CCCAAT17GENIChomozygous710120800
5151530016151530017CA23GENIChomozygous567721921
5151530452151530453TC37GENIChomozygous567721922
5151532097151532098AAT6GENIChomozygous710120802
5151532349151532350GA7GENIChomozygous567721923
5151532466151532467AT16GENIChomozygous567721924