chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43265050632650507GA4GENIChomozygous187102210
43265058632650587TA5GENIChomozygous187102211
43265069532650696AC19GENIChomozygous187102212
43265082232650823CT7GENIChomozygous187102213
43265098832650989GA17GENIChomozygous187102214
43265104432651045TG14GENIChomozygous187102215
43265123232651233CG14GENIChomozygous187102216
43265257532652576CT13GENIChomozygous187102217
43265411132654112TC19GENIChomozygous187102218
43265412232654123CT21GENIChomozygous187102219
43265427432654275CT23GENIChomozygous187102220
43265480732654808TC8GENIChomozygous187102221
43265552532655526CT10GENIChomozygous187102222
43265569532655696AG20GENIChomozygous187102223
43265577832655779TC18GENICpossibly homozygous187102224
43265580932655810CA19GENIChomozygous187102225
43265583632655837AT25GENIChomozygous187102226
43265597832655979CT19GENIChomozygous187102227
43265615132656152AC18GENIChomozygous187102228
43265615632656157AT19GENIChomozygous187102229
43265631232656313CT20GENIChomozygous187102230
43265667432656675TA19GENIChomozygous187102231
43265676132656762AG18GENIChomozygous187102232
43265694132656942GA18GENIChomozygous187102233