chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155681912155681913CT24GENIChomozygous57526702
4155682405155682406A-23GENIChomozygous57526704
4155682782155682783CT18GENIChomozygous57526706
4155683891155683892AG10GENIChomozygous57526708
4155683942155683943AG9GENIChomozygous57526710
4155684232155684233GA8GENIChomozygous57526712
4155686017155686018AG16GENIChomozygous57526714
4155686118155686119GA22GENIChomozygous57526716
4155688052155688053TC22GENICpossibly homozygous57526718
4155688174155688175GA17GENIChomozygous57526720
4155688536155688537GGTTTTTTTTT19GENIChomozygous57526722
4155688899155688901GG--11GENIChomozygous57526732
4155688902155688905TCG---11GENIChomozygous57526734
4155688949155688950CG12GENIChomozygous57526736
4155690175155690176AG11GENIChomozygous57526746
4155690744155690745AC10INTERGENIChomozygous57526748
4155688566155688567GGTTA12GENIChomozygous58287271