chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121371598613715987GC26INTERGENIChomozygous50281326
121371613413716135AG23INTERGENIChomozygous50281327
121371676613716767AG15INTERGENIChomozygous50281328
121371676913716770GA14INTERGENIChomozygous50281329
121371696313716964GT26INTERGENIChomozygous50281330
121371697713716978AC27INTERGENIChomozygous50281331
121371750713717518GACAACCAACA-----------19INTERGENIChomozygous50281332
121371752213717523GA18INTERGENIChomozygous50281333
121371757613717577GA6INTERGENIChomozygous50281334
121371761613717617CT4INTERGENICheterozygous50281335
121371796513717966C-3INTERGENICheterozygous50653812
121371697813716979AC27INTERGENIChomozygous50062164
121371774813717749AAT9INTERGENIChomozygous50062168
121371797113717972C-3INTERGENICheterozygous50653816
121371797613717977AAGT3INTERGENICheterozygous50653820
121371801213718013T-1INTERGENIChomozygous50062172
121371868413718685CT35INTERGENIChomozygous50281340
121371814113718224GTAGGCAAATGGTTGGAACTGGAAAATGTCATCTGAGTGAGGTAACCCAATCACAGAAAAACAGACATGGTATGCACTCATTG-----------------------------------------------------------------------------------14INTERGENICheterozygous50503875