chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101520757915207580CT55GENIChomozygous116737614
101520762015207621TC51GENICpossibly homozygous116497977
101520887415208875TC59GENIChomozygous116497983
101520921815209219CG51GENIChomozygous116497985
101520930615209307AG39GENIChomozygous116497987
101521158815211589GA46GENIChomozygous116737615
101520998015209980AAAA26GENICpossibly homozygous128791032
101520998615209986AAAC26GENICpossibly homozygous131088158