chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71261088812610889TC25GENIChomozygous53791320
71261160912611619AAAAAAAAAA----------7GENICpossibly homozygous55071104
71261388712613890CCT---12GENIChomozygous53791322
71261890012618901CA35GENIChomozygous53791325
71261968412619685GA30GENIChomozygous53791328
71262113712621138AAACACACAC8GENIChomozygous55071106
71262206112622062GA24GENIChomozygous53791330
71262213712622138CCAA11GENICheterozygous53791333
71262213712622138CCA11GENICheterozygous53791334
71262265912622660AG43GENIChomozygous53791336
71262432212624323CG20GENIChomozygous53791338
71262440312624404TTAG16GENIChomozygous53791340
71262442112624422TTA8GENIChomozygous55071108
71262576312625764A-10GENIChomozygous54630471
71261197712611978CT25GENIChomozygous54630457
71261306812613069GA22GENIChomozygous54630459
71262013812620139AG26GENIChomozygous54630461
71262098012620981CCT26GENIChomozygous54630463
71262391912623920GGC12GENIChomozygous54630465
71262459612624597GA13GENIChomozygous54630467
71262531212625314AG--18GENIChomozygous54630469
71262555312625554GGAAA4GENIChomozygous54954989
71261948112619482GGA12GENICpossibly homozygous54885005
71262627512626278GTC---13GENIChomozygous54630477