chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144271120142711202C-26GENIChomozygous49307377
144271120442711205CCA27GENIChomozygous49307378
144271138342711384AG29GENIChomozygous48685119
144271150142711502TC26GENIChomozygous48685120
144271160242711603CT31GENIChomozygous48685121
144271273542712736CA31GENIChomozygous48685122
144271283942712840TC27GENIChomozygous48685123
144271320942713210GT17GENIChomozygous48685124
144271371442713715AG24GENIChomozygous48685125
144271385942713860GT21GENIChomozygous48685126
144271447042714471AG14GENIChomozygous48685127
144271547842715479CG27GENIChomozygous48685128
144271556942715570CCTGTTGTTGTTGTTGT9GENICheterozygous49307379
144271556942715570CCTGTTGTTGTTGTTGTTGT9GENICpossibly homozygous49307380
144271581142715812GA26GENIChomozygous48685130
144271618042716181TC22GENIChomozygous48685131
144271720642717207CT33GENIChomozygous48685132
144271741242717413TC30GENIChomozygous48685133