chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121371598613715987GC8INTERGENIChomozygous50281326
121371613413716135AG10INTERGENIChomozygous50281327
121371676613716767AG12INTERGENIChomozygous50281328
121371676913716770GA12INTERGENIChomozygous50281329
121371696313716964GT14INTERGENIChomozygous50281330
121371697713716978AC16INTERGENIChomozygous50281331
121371697813716979AC17INTERGENIChomozygous50062164
121371750713717518GACAACCAACA-----------9INTERGENIChomozygous50281332
121371752213717523GA8INTERGENIChomozygous50281333
121371757613717577GA7INTERGENIChomozygous50281334
121371761613717617CT5INTERGENIChomozygous50281335
121371774813717749AAT3INTERGENIChomozygous50062168
121371868413718685CT11INTERGENIChomozygous50281340
121371822513718226TTAAGTGGCTATTA3INTERGENICheterozygous50556943
121371814113718224GTAGGCAAATGGTTGGAACTGGAAAATGTCATCTGAGTGAGGTAACCCAATCACAGAAAAACAGACATGGTATGCACTCATTG-----------------------------------------------------------------------------------4INTERGENICheterozygous50503875