chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
112534299725342998GA21GENIChomozygous115792315
112534309325343094CT29GENIChomozygous115792317
112534318825343189AC28GENIChomozygous115792319
112534382925343830CT24GENICpossibly homozygous115792321
112534434525344346TC20GENIChomozygous115792323
112534555425345555AG28GENIChomozygous115792325
112534763925347640AG19GENIChomozygous115792327
112534900525349006TG16GENIChomozygous115792329
112534919525349196AT12GENIChomozygous115792331
112534960925349610TC30GENIChomozygous115792333
112535033425350335CT24GENIChomozygous115792335
112535041725350418TC21GENIChomozygous115792337
112535059425350594GGTTAGAC18GENIChomozygous128892236
112535073725350737T35GENIChomozygous128892237
112535075625350759AGT32GENIChomozygous128892238
112535078525350786CT32GENIChomozygous115792339