chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109055976990559770CA5GENIChomozygous623016441
109055986290559863CT7GENIChomozygous623016442
109056012390560124GT12GENIChomozygous623016443
109056035790560360CCC---2GENICheterozygous740123547
109056081490560815CT13GENIChomozygous623016444
109056083390560834CT11GENIChomozygous623016445
109056092890560929CT17GENICheterozygous623016446
109056141190561412A-2GENIChomozygous740123548
109056164290561643GGAC8GENICpossibly homozygous740123550
109056223990562240GT3GENIChomozygous623016447
109056248190562482GT8GENICpossibly homozygous623016448
109056461790564618AC5GENIChomozygous623016449
109056464790564648CT10GENICpossibly homozygous623016450
109056468190564682AG12GENIChomozygous623016451
109056474790564748TC3GENIChomozygous623016452
109056480390564804GGGGGAATTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC2GENIChomozygous740123551
109056510390565104CT2GENIChomozygous623016453
109056510590565106TC2GENIChomozygous623016454
109056511690565117AG2GENIChomozygous623016455
109056512590565129GCTG----1GENIChomozygous740123552
109056519890565199GA10GENICheterozygous623016456
109056524390565244TC22GENIChomozygous623016457
109056527790565278CT15GENICpossibly homozygous623016458
109056542690565427AT19GENICheterozygous623016459
109056547590565476CT23GENIChomozygous623016460
109056586990565870GA9GENIChomozygous623016461