chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7131011172131011173GGA5GENIChomozygous54243946
7131011923131011924CG8GENICpossibly homozygous54243948
7131011953131011954CT4GENIChomozygous54243950
7131011984131011985AAACC1GENIChomozygous54113496
7131011987131011988CCAGG2GENICheterozygous54113498
7131012050131012051CT18GENIChomozygous54243954
7131012110131012111TC11GENIChomozygous54113499
7131012189131012193TTTT----7GENICheterozygous55031147
7131012190131012193TTT---7GENICheterozygous54243956
7131012261131012262A-16GENICpossibly homozygous54113501
7131013290131013291AAT1GENIChomozygous54113504
7131013501131013502AG16GENIChomozygous54113505
7131013642131013643CT12GENICheterozygous54522028
7131013739131013740GA12GENIChomozygous54113506
7131013917131013918AT19GENIChomozygous54113507