chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227429473227429474GC30GENIChomozygous108559218
1227429643227429644AC20GENIChomozygous108559219
1227430046227430047TC18GENIChomozygous108559220
1227430337227430338TC20GENIChomozygous108559221
1227430355227430356CT23GENIChomozygous108559222
1227430385227430386CT25GENIChomozygous108559223
1227430596227430597AG35GENIChomozygous108559224
1227430721227430722AG29GENIChomozygous108559225
1227430729227430730AG27GENIChomozygous108559226
1227431045227431046TC24GENIChomozygous108559228
1227431460227431461CA35GENIChomozygous108559229
1227431634227431635TC19GENIChomozygous108559230
1227431795227431796AT15GENIChomozygous108559231
1227431973227431974TC13GENIChomozygous108559232
1227432241227432242TC18GENIChomozygous108559233
1227432281227432282GC26GENIChomozygous108559234
1227432968227432969GT33GENIChomozygous108559235
1227434405227434406AG17GENIChomozygous108559237
1227434406227434407CG16GENIChomozygous108559238
1227434502227434503GA12GENIChomozygous108559239
1227435250227435251TC14GENIChomozygous108559241
1227436152227436153TC33GENIChomozygous108559242
1227436174227436175AG29GENIChomozygous108559243
1227437038227437039TC20GENIChomozygous108559244
1227437039227437040TG19GENIChomozygous108559245
1227437898227437899CG16GENIChomozygous108559246
1227439268227439269AT31GENIChomozygous108559247
1227439444227439445TG19GENIChomozygous108559248
1227439680227439681CT21GENIChomozygous108559249
1227439916227439917TC18GENIChomozygous108559250
1227440363227440364CA32GENIChomozygous108559251
1227440669227440670TC33GENIChomozygous108559252