chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139190510139190511CT31GENICpossibly homozygous55748920
5139191548139191549TC12GENIChomozygous55748921
5139191791139191792GA16GENIChomozygous55748922
5139192271139192272TTA12GENIChomozygous55748923