chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153174577431745775AG19GENICpossibly homozygous403379549
153174577431745775A19GENICheterozygous403379550
153174578431745785AG36GENIChomozygous403379551
153174578431745785A36GENICheterozygous403379552
153174578831745789A35GENIChomozygous403379553
153174578831745789AG35GENICheterozygous403379554
153174580431745805AG36GENIChomozygous139709032
153174581031745811C35GENIChomozygous403379555
153174581031745811CG35GENICheterozygous403379556
153174584931745850GA28GENIChomozygous403379557
153174584931745850G28GENICheterozygous403379558
153179082731790828AT29GENIChomozygous139709036
153177531331775313A17GENICheterozygous140916140
153174581031745813CAG35GENIChomozygous139626389
153179812831798129A21GENIChomozygous139626390