chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4181663939181663940CA39GENIChomozygous112977132
4181664390181664391CG36GENIChomozygous112977133
4181664418181664419TC39GENIChomozygous112977134
4181664626181664627CT57GENIChomozygous112977135
4181664926181664927CA42GENIChomozygous112977136
4181669097181669098GA32GENIChomozygous112977137
4181669740181669741CT50GENIChomozygous112977138
4181670169181670170GA57GENIChomozygous112977139
4181670719181670720CA46GENIChomozygous112977140
4181670843181670844TG49GENIChomozygous112977141
4181671222181671223TA38GENIChomozygous112977142
4181671417181671418AC36GENIChomozygous112977143
4181671947181671948AT46GENIChomozygous112977144
4181672149181672150AG57GENIChomozygous112977145
4181672835181672836CT36GENIChomozygous112977146