chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104511089145110892CG47GENIChomozygous51872756
104511184845111849GA28GENICpossibly homozygous52244821
104511215645112157GA28GENIChomozygous52244823
104511217045112171CA29GENIChomozygous51872760
104511217645112177TTG29GENIChomozygous51441737
104511235145112352CT33GENIChomozygous52244825
104511327445113275TC33GENIChomozygous51441740