chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4181663939181663940CA17GENIChomozygous112977132
4181664390181664391CG19GENIChomozygous112977133
4181664418181664419TC16GENIChomozygous112977134
4181664626181664627CT20GENIChomozygous112977135
4181664926181664927CA24GENIChomozygous112977136
4181667628181667629AG36GENIChomozygous113567539
4181669097181669098GA14GENIChomozygous112977137
4181669740181669741CT16GENIChomozygous112977138
4181670169181670170GA25GENIChomozygous112977139
4181670719181670720CA25GENIChomozygous112977140
4181670843181670844TG33GENIChomozygous112977141
4181671222181671223TA24GENIChomozygous112977142
4181671417181671418AC29GENIChomozygous112977143
4181671947181671948AT23GENIChomozygous112977144
4181672149181672150AG20GENIChomozygous112977145
4181672835181672836CT14GENIChomozygous112977146