chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227429473227429474GC33GENIChomozygous108559218
1227429643227429644AC46GENIChomozygous108559219
1227430046227430047TC36GENIChomozygous108559220
1227430385227430386CT27GENIChomozygous108559223
1227430596227430597AG32GENIChomozygous108559224
1227430721227430722AG21GENIChomozygous108559225
1227430729227430730AG22GENIChomozygous108559226
1227430874227430875AG28GENIChomozygous108559227
1227431045227431046TC22GENIChomozygous108559228
1227431460227431461CA29GENIChomozygous108559229
1227431634227431635TC33GENIChomozygous108559230
1227431795227431796AT39GENIChomozygous108559231
1227431973227431974TC37GENIChomozygous108559232
1227432281227432282GC43GENIChomozygous108559234
1227432968227432969GT23GENIChomozygous108559235
1227433338227433339CT33GENIChomozygous108559236
1227434502227434503GA32GENIChomozygous108559239
1227435250227435251TC37GENIChomozygous108559241
1227436174227436175AG35GENIChomozygous108559243
1227437038227437039TC29GENIChomozygous108559244
1227437039227437040TG29GENIChomozygous108559245
1227437898227437899CG32GENIChomozygous108559246
1227439268227439269AT33GENIChomozygous108559247
1227439680227439681CT35GENIChomozygous108559249
1227439916227439917TC38GENIChomozygous108559250
1227440363227440364CA24GENIChomozygous108559251
1227440669227440670TC25GENIChomozygous108559252
1227438054227438055GA53GENIChomozygous108999185