chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104633046446330465AG68GENIChomozygous116772548
104633060546330606AG70GENICpossibly homozygous116772550
104633265246332653AG84GENIChomozygous116877713
104633165246331653CG83GENIChomozygous116877705
104633202646332027GA77GENIChomozygous116877707
104633208946332090AG82GENIChomozygous116877709
104633253546332536AT73GENIChomozygous116877711
104633167346331684CCCTGTCGGTC79GENIChomozygous131092542
104633276346332764TC61GENIChomozygous116772552
104633390446333905GA73GENIChomozygous116772554
104633432046334321AG73GENIChomozygous116772556
104633454146334542GC39GENIChomozygous116772558
104633457546334576C39GENIChomozygous131092543
104633494946334950TC56GENIChomozygous116772560
104633527446335275AG60GENIChomozygous116772562
104633535746335358TA61GENIChomozygous116772564
104633542846335429CT71GENIChomozygous116772566
104633587846335879AG81GENIChomozygous116772568
104633605946336060GA68GENIChomozygous116772570
104633649046336491GA70GENICpossibly homozygous116772572
104633554246335543TC72GENIChomozygous116585679
104633913746339138AG60GENIChomozygous116772576
104633694146336942CT70GENIChomozygous116585685
104633859046338591CT65GENIChomozygous116772574
104633912546339126AG62GENIChomozygous116585687