chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107997295979972960CT58GENIChomozygous138831057
107997297579972976CA53GENIChomozygous138831058
107997317579973176AT56GENIChomozygous138831059
107997397979973980TC53GENIChomozygous138831060
107997499179974992GA61GENIChomozygous138831061
107997689879976898TG45GENICpossibly homozygous138693285
107997714079977141TC50GENIChomozygous138831062
107997863179978632TC55GENIChomozygous138831063
107997878279978783AT56GENIChomozygous138831064
107998131379981314GA59GENICpossibly homozygous138831068
107997926679979267CT55GENIChomozygous138831065
107998008879980089GT75GENIChomozygous138831066
107998019679980197TA59GENIChomozygous138831067
107998274079982741CT61GENIChomozygous138831069
107998321179983212TC60GENIChomozygous138831070
107998378079983781TC56GENIChomozygous138831071
107998381879983819AG46GENIChomozygous138831072
107998585579985856GA58GENIChomozygous138831073