chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119048698690486987GA23GENIChomozygous51035439
119048771290487722ACACACACAC----------11GENIChomozygous50863619
119048827990488280CCA6GENICheterozygous50863620
119048827990488280CCAAA6GENICheterozygous51035440
119048852890488529GA15GENIChomozygous51135197
119048865990488665CCTCTC------7GENIChomozygous51135200
119048897290488978CTCTCT------7GENICheterozygous51197691
119048916690489167CG24GENIChomozygous51035442
119048918990489191AC--15GENIChomozygous51035443
119048932090489321CG18GENIChomozygous50974787
119049031690490317GA28GENIChomozygous50974788
119049127790491278AAGAGTCTGAGAG26GENIChomozygous50863626
119049361490493615CT24GENIChomozygous50974790
119049385490493855CT17GENIChomozygous51135203
119049537790495378TC16GENIChomozygous50863632
119049627890496279CT15GENIChomozygous50974793
119049629790496298AG12GENIChomozygous50974794
119049473590494765GAAGCTCCCCCTCCAGTCAGGCCCTGCTCT------------------------------4GENIChomozygous51192901
119048896890488978CTCTCTCTCT----------7GENICpossibly homozygous51192899
119049472990494731CC--4GENIChomozygous51192900