chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84550982945509830CT42GENIChomozygous52617279
84550983345509834AT40GENIChomozygous52617281
84550988845509889TC40GENIChomozygous52617283
84550994345509944CT38GENIChomozygous52617285
84550994645509947GA38GENIChomozygous52617287
84551002845510029TTG24GENIChomozygous52617289
84551016545510166GA23GENIChomozygous52617291
84551024645510247GC29GENIChomozygous52617293
84551047345510474AT12GENIChomozygous52617295
84551058445510585CT24GENIChomozygous52617297
84551088145510882CT22GENIChomozygous52617299
84551090345510904CT18GENIChomozygous52617301
84551145745511458TC23GENIChomozygous52617303
84551146745511468GA23GENICpossibly homozygous52617305
84551151745511518TC35GENIChomozygous52617307
84551167545511676AG21GENIChomozygous52617309
84551178045511781AG27GENIChomozygous52617311
84551180245511803G-31GENIChomozygous52617313
84551181845511819TC32GENIChomozygous52617315