chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173046883130468832TC37GENIChomozygous111022351
173046902430469025GA33GENIChomozygous111022355
173046925430469255GT14GENIChomozygous111022357
173046931130469312GC16GENIChomozygous111022359
173046951530469516TC26GENIChomozygous111241707
173046968730469688AG23GENIChomozygous111241709
173046993930469940CA22GENIChomozygous111241711
173047001630470017AC27GENIChomozygous111241713
173047017230470173TG37GENIChomozygous111022361
173047019930470200TG38GENIChomozygous111241715
173047030130470302CT29GENIChomozygous111022367
173047030930470310GC29GENIChomozygous111241716
173047035830470359TC25GENIChomozygous111022369
173047038630470387GA30GENICheterozygous119360521
173047064530470646TC23GENICpossibly homozygous111022371
173047244830472449TC22GENIChomozygous111022373
173047323930473240GA24GENIChomozygous111241718
173047407830474079TC24GENIChomozygous111022375