chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144271120142711202CCA38GENIChomozygous48685117
144271120442711205C-39GENIChomozygous48685118
144271138342711384AG37GENIChomozygous48685119
144271150142711502TC34GENIChomozygous48685120
144271230442712305AG54GENIChomozygous49178650
144271273542712736CA30GENIChomozygous48685122
144271283942712840TC33GENICpossibly homozygous48685123
144271359442713595TC29GENICpossibly homozygous49178651
144271371442713715AG44GENIChomozygous48685125
144271387042713871TTA46GENIChomozygous49178652
144271447042714471AG36GENIChomozygous48685127
144271611242716115GGG---18GENIChomozygous49178653
144271615742716158CT28GENIChomozygous49178654
144271618042716181TC36GENIChomozygous48685131
144271682642716827A-45GENIChomozygous49178655
144271688242716883CA39GENIChomozygous49178656
144271694742716948GA42GENIChomozygous49178657
144271741242717413TC33GENICpossibly homozygous48685133
144271858742718588TA43GENIChomozygous49178658