chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
478533517853352GA16GENIChomozygous946583254
478534947853495CT20GENIChomozygous946583255
478535147853515TC17GENIChomozygous946583256
478539867853987AG9GENIChomozygous946583257
478542197854220GA26GENIChomozygous946583258
478542657854266AG34GENIChomozygous946583259
478544197854420AG22GENIChomozygous946583260
478555177855518TC41GENIChomozygous946583261
478571537857154GA25GENIChomozygous946583262
478582177858218GA34GENICpossibly homozygous946583263
478595507859551CT20GENIChomozygous946583264
478600687860069CT24GENIChomozygous946583265
478626537862654TC16GENIChomozygous946583266
478627687862769CT26GENIChomozygous946583267
478631467863147TC21GENIChomozygous946583268
478640597864060TC14GENIChomozygous946583269
478644567864457AG17GENIChomozygous946583270
478646587864659TA24GENIChomozygous946583271
478657907865791CT15GENIChomozygous946583272
478663567866357GA19GENIChomozygous946583273
478666637866664CT30GENIChomozygous946583274
478692267869227TA19GENIChomozygous946583275
478692277869228AT19GENIChomozygous946583276
478744457874446GC13GENIChomozygous946583277
478755057875506CT30GENIChomozygous946583278
478758067875807CT17GENIChomozygous946583279
478758117875812GA18GENIChomozygous946583280
478786767878677CT14GENIChomozygous946583281
478800267880027GC21GENIChomozygous946583282
478800717880072TA20GENIChomozygous946583283
478801017880102TA20GENIChomozygous946583284
478801047880105GC20GENIChomozygous946583285