chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144271150142711502TC23GENIChomozygous48685120
144271175342711754TTAC7GENICheterozygous49396705
144271230442712305AG27GENIChomozygous49178650
144271273542712736CA29GENIChomozygous48685122
144271283942712840TC21GENIChomozygous48685123
144271359442713595TC32GENIChomozygous49178651
144271371442713715AG21GENIChomozygous48685125
144271387042713871TTA27GENICpossibly homozygous49178652
144271447042714471AG25GENIChomozygous48685127
144271611242716115GGG---23GENIChomozygous49178653
144271615742716158CT20GENIChomozygous49178654
144271618042716181TC18GENIChomozygous48685131
144271682642716827A-7GENIChomozygous49178655
144271688242716883CA13GENIChomozygous49178656
144271694742716948GA17GENIChomozygous49178657
144271741242717413TC25GENIChomozygous48685133
144271858742718588TA20GENIChomozygous49178658