chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4181663939181663940CA18GENIChomozygous112977132
4181664390181664391CG13GENIChomozygous112977133
4181664418181664419TC13GENIChomozygous112977134
4181664626181664627CT19GENIChomozygous112977135
4181664926181664927CA16GENIChomozygous112977136
4181669097181669098GA9GENIChomozygous112977137
4181669740181669741CT14GENIChomozygous112977138
4181670169181670170GA15GENIChomozygous112977139
4181670719181670720CA14GENIChomozygous112977140
4181670843181670844TG10GENIChomozygous112977141
4181671222181671223TA14GENICpossibly homozygous112977142
4181671417181671418AC14GENIChomozygous112977143
4181671947181671948AT16GENIChomozygous112977144
4181672149181672150AG17GENIChomozygous112977145
4181672835181672836CT23GENIChomozygous112977146