chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99423873494238735TC27GENIChomozygous803919503
99423878194238782TC44GENIChomozygous803919504
99423891794238918GA30GENIChomozygous803919505
99423896394238964AG20GENIChomozygous803919506
99423900194239002CT26GENIChomozygous803919507
99423913494239135GA34GENIChomozygous803919508
99423918894239189TC35GENIChomozygous803919509
99423932694239327GA30GENIChomozygous803919510
99424098994240990CT29GENICpossibly homozygous803919511
99424207294242073GC32GENIChomozygous803919512
99424233294242333AG27GENIChomozygous803919513
99424236494242365AC30GENIChomozygous803919514
99424429794244298GC23GENIChomozygous803919515
99424750794247508GA26GENIChomozygous803919516
99424763094247631AC37GENIChomozygous803919517
99424796994247970AG31GENIChomozygous803919518
99424805794248058AT21GENIChomozygous803919519
99424848494248485CG41GENIChomozygous803919520
99424942394249424TC20GENIChomozygous803919521
99425083194250832CT36GENIChomozygous803919522
99425212494252125AG39INTERGENIChomozygous803919523