chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141286859141286860AACTGCTGCCCCTG19GENIChomozygous54158242
7141287908141287909AC31GENIChomozygous54158247
7141288226141288227TC49GENIChomozygous54158248
7141287086141287087GA21GENICheterozygous54265721
7141288837141288838TC27GENIChomozygous54265724
7141287019141287020G-23GENIChomozygous54265714
7141287081141287082AACTCTAAGGTATG13GENIChomozygous54265718
7141289801141289802GT11GENIChomozygous54265730
7141292784141292785AG24GENIChomozygous54265733
7141293279141293280AG41GENIChomozygous54158267
7141292400141292401AAC15GENICheterozygous54529571