chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151525906151525907GT2GENIChomozygous631130368
5151526224151526225AG14GENIChomozygous631130369
5151526927151526928GC18GENICpossibly homozygous631130370
5151527609151527610CCTTTTTTTTTT1GENIChomozygous745554065
5151527853151527854CT3GENICheterozygous631130371
5151528329151528330GA7GENICheterozygous631130372
5151529328151529329CCCAATCAAT4GENIChomozygous745554067
5151530016151530017CA18GENIChomozygous631130373
5151530452151530453TC16GENIChomozygous631130374
5151532097151532098AAT2GENIChomozygous745554068
5151532349151532350GA24GENIChomozygous631130375
5151532466151532467AT13GENIChomozygous631130376