chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157127932157127933CT32GENIChomozygous112905477
4157128941157128942TG16GENIChomozygous112905479
4157129150157129151AG16GENIChomozygous112905481
4157129153157129154GC14GENIChomozygous112905483
4157129293157129294TG13GENIChomozygous112905485
4157130255157130256AG12GENIChomozygous112905487
4157130302157130303GA17GENIChomozygous112905489
4157130649157130650CG18GENIChomozygous112905491
4157131094157131095TA28GENIChomozygous112905493
4157132353157132354AG17GENIChomozygous112905495
4157132776157132777TG25GENIChomozygous112905497
4157133713157133714CT20GENIChomozygous112905499
4157133758157133759CT19GENICpossibly homozygous112905501
4157134281157134282TA29GENIChomozygous112905507
4157134353157134354TC32GENIChomozygous112905509
4157134471157134472AT20GENIChomozygous112905511
4157134715157134716GA26GENIChomozygous112905513