chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144271150142711502TC47GENIChomozygous48685120
144271160242711603CT50GENIChomozygous48685121
144271273542712736CA43GENIChomozygous48685122
144271283942712840TC50GENIChomozygous48685123
144271320942713210GT39GENIChomozygous48685124
144271371442713715AG39GENIChomozygous48685125
144271385942713860GT33GENIChomozygous48685126
144271447042714471AG48GENIChomozygous48685127
144271547842715479CG48GENIChomozygous48685128
144271556942715570CCTGT8GENIChomozygous48685129
144271581142715812GA52GENIChomozygous48685130
144271618042716181TC35GENIChomozygous48685131
144271720642717207CT37GENIChomozygous48685132
144271741242717413TC56GENIChomozygous48685133