chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107997295979972960CT49GENIChomozygous138831057
107997297579972976CA50GENICpossibly homozygous138831058
107997317579973176AT53GENIChomozygous138831059
107997397979973980TC57GENIChomozygous138831060
107997714079977141TC41GENIChomozygous138831062
107997863179978632TC46GENIChomozygous138831063
107997878279978783AT45GENIChomozygous138831064
107997926679979267CT63GENIChomozygous138831065
107998008879980089GT47GENIChomozygous138831066
107998019679980197TA54GENIChomozygous138831067
107998131379981314GA57GENIChomozygous138831068
107997689879976898TG27GENICpossibly homozygous138693285
107997659379976661ATGTGTATATGTGTGTATGTATATAAGTGTGTGTATATGTGTATGTATGTGTATGTATATATGTGTAC43GENIChomozygous144857139