chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153771592137715922T16GENICheterozygous131159481
153774590737745907T16GENICpossibly homozygous129246377
153777002937770031TG16GENICheterozygous130789127
153778163937781639G7GENIChomozygous130149008
153778168137781682T4GENIChomozygous130149009
153778169637781699CTA4GENIChomozygous130149010
153778172637781729CAA4GENIChomozygous130149011
153778173537781736T4GENIChomozygous130149012
153778174837781749C4GENIChomozygous130149013
153778175137781752T3GENIChomozygous130149014
153778176337781764A2GENIChomozygous130440407
153778205937782060T9GENIChomozygous130592485
153778208037782081C8GENIChomozygous130592486