chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101527457715274578CA18GENIChomozygous138726809
101527544515275446TC16GENIChomozygous138726810
101527612215276123CT22GENIChomozygous138726811
101527629215276293CT15GENIChomozygous138726812
101527708215277083T12GENIChomozygous138669290
101527710215277103TC12GENIChomozygous138726813
101527755815277559AG14GENIChomozygous138726814
101528202915282030A19GENICpossibly homozygous138669291
101528434315284344CT15GENIChomozygous138726815
101529159615291597AG19GENIChomozygous138726817
101529423815294239CT26GENIChomozygous138726818
101530087115300872G16GENICpossibly homozygous138669293
101530281515302816AG25GENIChomozygous138726819
101528052115280521TA3GENIChomozygous142197123
101528121415281215TC2GENIChomozygous142219428
101530247015302471GC5GENICheterozygous142219429
101530247315302474GC6GENICheterozygous142219430