chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182933097229330973CT24GENIChomozygous110318197
182933178329331784GC18GENIChomozygous110318201
182933223129332232GC17GENIChomozygous110318203
182933251129332512GC6GENIChomozygous110456477
182933311829333119CG22GENIChomozygous110318205
182933334529333346GA20GENIChomozygous110318207
182933352129333522GC19GENIChomozygous110318209
182933406129334062AG10GENIChomozygous110318211
182933547529335476GA21GENICpossibly homozygous110318213
182933624329336244CT19GENIChomozygous110456478
182933685429336855TG14GENIChomozygous110318217
182933694129336942CT12GENIChomozygous110456479
182933807929338080GT21GENIChomozygous110318219
182933920429339205TC18GENIChomozygous110318221
182933942329339424CG16GENIChomozygous110456480
182933960829339609TA17GENIChomozygous110318223
182934018229340183GA21GENIChomozygous110318225
182933984829339849GA21GENIChomozygous110723551
182933406529334072AACTTCC9GENIChomozygous129527264
182933574529335745G22GENIChomozygous129527265
182933829429338295C21GENIChomozygous129527266
182933942329339423G16GENIChomozygous129527267
182933941129339411T13GENICheterozygous132361852