chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4181663939181663940CA39GENIChomozygous112977132
4181664390181664391CG49GENIChomozygous112977133
4181664418181664419TC51GENIChomozygous112977134
4181664626181664627CT64GENIChomozygous112977135
4181664926181664927CA52GENIChomozygous112977136
4181669097181669098GA39GENIChomozygous112977137
4181669740181669741CT48GENIChomozygous112977138
4181670169181670170GA67GENIChomozygous112977139
4181670719181670720CA46GENIChomozygous112977140
4181670843181670844TG48GENIChomozygous112977141
4181671222181671223TA46GENIChomozygous112977142
4181671417181671418AC39GENIChomozygous112977143
4181671947181671948AT46GENIChomozygous112977144
4181672149181672150AG70GENIChomozygous112977145
4181672835181672836CT42GENIChomozygous112977146