chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140465355140465356CT69GENIChomozygous115938718
7140465548140465549GT47GENIChomozygous115938719
7140465585140465586CT52GENIChomozygous115938720
7140468408140468408TTC47GENICpossibly homozygous128529079
7140465828140465832GGTG50GENIChomozygous128529078