chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121416674914166750TC28GENIChomozygous115445268
121416675614166757TG26GENIChomozygous115445270
121416676014166761GC22GENIChomozygous115445272
121416676114166762GC22GENIChomozygous115445274
121416677314166774CG21GENIChomozygous115445277
121416678114166782CG19GENIChomozygous115262331
121416678814166789GA19GENIChomozygous115445279
121416682414166825GC17GENIChomozygous115445281
121416835514168356CT22GENIChomozygous115262337
121416862914168630TC33GENIChomozygous115262339
121416893214168933CT34GENIChomozygous115262341
121417527614175277CA27GENIChomozygous115262347
121417573714175738AG44GENIChomozygous115262349