chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108213131982131320G-21GENIChomozygous51516668
108213134682131347C-19GENIChomozygous51516669
108213449582134496GT12GENIChomozygous51516690
108213769082137691C-7GENICpossibly homozygous51516710
108213897882138979GT14GENIChomozygous51516720
108213898382138984CT15GENIChomozygous51516721
108213899882138999GT13GENIChomozygous51516722
108213900082139001AT14GENIChomozygous51516723
108213900782139008AT13GENIChomozygous51516724
108213901982139020AT16GENIChomozygous51516725
108213925882139259CG17GENIChomozygous51516729
108213926282139263AAG19GENIChomozygous51516730
108213926882139269A-19GENIChomozygous51516731
108213447482134476TT--7GENICheterozygous52390722
108213463682134638TG--3GENICheterozygous52390724
108213896182138962GT14GENICpossibly homozygous52390726
108216039082160391TG19INTERGENIChomozygous51516792
108216039182160392TA19INTERGENIChomozygous51516793
108216039682160397C-19INTERGENIChomozygous51516794
108216039782160398CG19INTERGENIChomozygous52390728
108216161582161616G-31INTERGENICheterozygous51516802
108216167882161679T-38INTERGENICheterozygous52390730
108216397582163976CT27INTERGENICheterozygous51516809
108217032182170325TATG----13INTERGENIChomozygous51717210
108217776782177768CCT1GENIChomozygous52390732
108218548182185482CCA35GENIChomozygous51516834