chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4181664390181664391CG38GENIChomozygous112977133
4181664418181664419TC36GENIChomozygous112977134
4181664626181664627CT21GENIChomozygous112977135
4181664926181664927CA31GENIChomozygous112977136
4181667628181667629AG16GENIChomozygous113567539
4181669097181669098GA28GENIChomozygous112977137
4181669740181669741CT16GENIChomozygous112977138
4181670169181670170GA16GENIChomozygous112977139
4181670719181670720CA39GENIChomozygous112977140
4181670843181670844TG26GENIChomozygous112977141
4181671222181671223TA14GENIChomozygous112977142
4181671417181671418AC27GENIChomozygous112977143
4181671947181671948AT15GENIChomozygous112977144
4181672149181672150AG20GENIChomozygous112977145
4181672835181672836CT32GENIChomozygous112977146
4181665147181665148GA16GENIChomozygous119457747