chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71261088812610889TC31GENIChomozygous53791320
71261160912611619AAAAAAAAAA----------7GENICpossibly homozygous55071104
71261197712611978CT28GENIChomozygous54630457
71261306812613069GA26GENIChomozygous54630459
71261388712613890CCT---29GENIChomozygous53791322
71261890012618901CA51GENICpossibly homozygous53791325
71261948112619482GGA16GENICheterozygous54885005
71261968412619685GA49GENIChomozygous53791328
71262013812620139AG37GENIChomozygous54630461
71262098012620981CCT38GENICpossibly homozygous54630463
71262113712621138AAACACACAC16GENIChomozygous55071106
71262206112622062GA37GENIChomozygous53791330
71262213712622138CCAA27GENICheterozygous53791333
71262213712622138CCA27GENICheterozygous53791334
71262265912622660AG40GENICpossibly homozygous53791336
71262391912623920GGC21GENIChomozygous54630465
71262432212624323CG19GENIChomozygous53791338
71262440312624404TTAG21GENIChomozygous53791340
71262442112624422TTA24GENICheterozygous55071108
71262459612624597GA29GENICpossibly homozygous54630467
71262531212625314AG--23GENIChomozygous54630469
71262555312625554GGAAA7GENICpossibly homozygous54954989
71262576312625764A-9GENIChomozygous54630471
71262627512626278GTC---21GENIChomozygous54630477
71262746812627469TC7GENICheterozygous53791361