chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144271138342711384AG19GENICpossibly homozygous48685119
144271150142711502TC7GENIChomozygous48685120
144271230442712305AG15GENIChomozygous49178650
144271273542712736CA11GENIChomozygous48685122
144271283942712840TC15GENIChomozygous48685123
144271359442713595TC12GENICpossibly homozygous49178651
144271371442713715AG17GENIChomozygous48685125
144271447042714471AG20GENIChomozygous48685127
144271611242716115GGG---6GENICheterozygous49178653
144271615742716158CT9GENIChomozygous49178654
144271618042716181TC10GENICheterozygous48685131
144271682642716827A-5GENIChomozygous49178655
144271688242716883CA2GENIChomozygous49178656
144271694742716948GA14GENIChomozygous49178657
144271741242717413TC8GENICpossibly homozygous48685133
144271858742718588TA20GENIChomozygous49178658