chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182770076027700761CT16GENIChomozygous814347225
182770796427707965AG15GENIChomozygous814347226
182771117527711176AC2GENIChomozygous814347227
182771309527713096CT41GENIChomozygous814347228
182771722827717229AG21GENIChomozygous814347229
182771762527717626AG12GENIChomozygous814347230
182771907027719071AG16GENIChomozygous814347231
182771910927719110AC19GENIChomozygous814347232
182772036227720363TC25GENIChomozygous814347233
182772072327720724AG17GENIChomozygous814347234
182772109227721093CT25GENIChomozygous814347235
182772293527722936GA32GENIChomozygous814347236
182772317627723177CT36GENICpossibly homozygous814347237
182772434427724345TC25GENIChomozygous814347238
182772456427724565TC12GENIChomozygous814347239