chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121371598613715987GC35INTERGENIChomozygous50281326
121371613413716135AG34INTERGENICpossibly homozygous50281327
121371676613716767AG35INTERGENIChomozygous50281328
121371676913716770GA37INTERGENIChomozygous50281329
121371696313716964GT29INTERGENIChomozygous50281330
121371697713716978AC32INTERGENIChomozygous50281331
121371697813716979AC33INTERGENIChomozygous50062164
121371750713717518GACAACCAACA-----------14INTERGENICpossibly homozygous50281332
121371752213717523GA10INTERGENIChomozygous50281333
121371757613717577GA15INTERGENIChomozygous50281334
121371761613717617CT14INTERGENIChomozygous50281335
121371796513717966C-19INTERGENIChomozygous50653812
121371797113717972C-22INTERGENIChomozygous50653816
121371797613717977AAGT22INTERGENIChomozygous50653820
121371801213718013T-23INTERGENIChomozygous50062172
121371805013718052CC--20INTERGENIChomozygous50692251
121371805213718053TTTC20INTERGENIChomozygous50692254
121371812913718138TTTATGAAA---------3INTERGENICheterozygous50748179
121371868413718685CT25INTERGENIChomozygous50281340
121371814113718224GTAGGCAAATGGTTGGAACTGGAAAATGTCATCTGAGTGAGGTAACCCAATCACAGAAAAACAGACATGGTATGCACTCATTG-----------------------------------------------------------------------------------8INTERGENICheterozygous50503875