chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4177467434177467437TCC---12GENICheterozygous58822022
4177467442177467444TC--10GENICheterozygous58822024
4177467443177467444CCGGGGGG10GENICheterozygous58822026
4177467448177467451CCA---12GENICheterozygous58822028
4177467452177467453C-14GENICheterozygous58822030
4177472833177472834AAG32GENIChomozygous57015899
4177479785177479786GGA12GENICheterozygous58483878
4177479786177479787A-12GENICheterozygous58483879
4177479844177479845G-9GENICheterozygous58445900
4177485844177485845CCTGTG5GENIChomozygous58357903
4177490282177490283TTTG4GENICheterozygous58408596
4177490283177490285TG--4GENICheterozygous58529856
4177493265177493266CCA9GENICpossibly homozygous58357905
4177494164177494166GA--12GENICheterozygous58597133
4177509065177509067AC--27GENICheterozygous58445904