chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144271120142711202C-28GENIChomozygous49307377
144271120442711205CCA28GENIChomozygous49307378
144271138342711384AG31GENIChomozygous48685119
144271150142711502TC29GENIChomozygous48685120
144271175342711754TTAC1GENIChomozygous49396705
144271230442712305AG23GENIChomozygous49178650
144271273542712736CA36GENIChomozygous48685122
144271283942712840TC26GENIChomozygous48685123
144271359442713595TC24GENIChomozygous49178651
144271371442713715AG27GENIChomozygous48685125
144271387042713871TTA21GENIChomozygous49178652
144271447042714471AG23GENIChomozygous48685127
144271611242716115GGG---18GENIChomozygous49178653
144271615742716158CT25GENIChomozygous49178654
144271618042716181TC26GENIChomozygous48685131
144271682642716827A-16GENICpossibly homozygous49178655
144271688242716883CA25GENIChomozygous49178656
144271694742716948GA28GENIChomozygous49178657
144271741242717413TC33GENIChomozygous48685133
144271858742718588TA28GENIChomozygous49178658