chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104633046446330465AG56GENIChomozygous116772548
104633060546330606AG47GENIChomozygous116772550
104633265246332653AG57GENIChomozygous116877713
104633165246331653CG71GENIChomozygous116877705
104633202646332027GA68GENIChomozygous116877707
104633208946332090AG64GENIChomozygous116877709
104633253546332536AT68GENICpossibly homozygous116877711
104633276346332764TC50GENIChomozygous116772552
104633390446333905GA49GENIChomozygous116772554
104633432046334321AG50GENIChomozygous116772556
104633454146334542GC50GENIChomozygous116772558
104633494946334950TC60GENIChomozygous116772560
104633527446335275AG54GENIChomozygous116772562
104633535746335358TA62GENIChomozygous116772564
104633542846335429CT65GENIChomozygous116772566
104633587846335879AG67GENIChomozygous116772568
104633605946336060GA68GENIChomozygous116772570
104633649046336491GA56GENIChomozygous116772572
104633694146336942CT57GENIChomozygous116585685
104633167346331684CCCTGTCGGTC61GENIChomozygous131092542
104633457546334576C57GENIChomozygous131092543
104633554246335543TC50GENIChomozygous116585679
104633859046338591CT56GENIChomozygous116772574
104633912546339126AG54GENIChomozygous116585687
104633913746339138AG49GENIChomozygous116772576