chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227429473227429474GC21GENIChomozygous108559218
1227429643227429644AC28GENIChomozygous108559219
1227430046227430047TC27GENIChomozygous108559220
1227430337227430338TC16GENIChomozygous108559221
1227430355227430356CT15GENIChomozygous108559222
1227430385227430386CT22GENIChomozygous108559223
1227430596227430597AG29GENIChomozygous108559224
1227430721227430722AG23GENIChomozygous108559225
1227430729227430730AG24GENIChomozygous108559226
1227430874227430875AG31GENIChomozygous108559227
1227431045227431046TC27GENIChomozygous108559228
1227431155227431155T27GENIChomozygous127488203
1227431460227431461CA28GENIChomozygous108559229
1227431634227431635TC28GENIChomozygous108559230
1227431795227431796AT21GENIChomozygous108559231
1227431973227431974TC24GENIChomozygous108559232
1227432241227432242TC20GENIChomozygous108559233
1227432281227432282GC20GENIChomozygous108559234
1227432968227432969GT22GENIChomozygous108559235
1227433338227433339CT19GENIChomozygous108559236
1227434140227434140A24GENICpossibly homozygous127488205
1227434405227434406AG17GENIChomozygous108559237
1227434406227434407CG17GENIChomozygous108559238
1227434502227434503GA34GENIChomozygous108559239
1227435250227435251TC29GENIChomozygous108559241
1227436174227436175AG24GENIChomozygous108559243
1227437038227437039TC21GENIChomozygous108559244
1227437039227437040TG21GENIChomozygous108559245
1227437898227437899CG29GENIChomozygous108559246
1227439268227439269AT30GENIChomozygous108559247
1227439444227439445TG21GENIChomozygous108559248
1227439680227439681CT27GENIChomozygous108559249
1227439916227439917TC38GENIChomozygous108559250
1227440363227440364CA18GENIChomozygous108559251
1227440669227440670TC20GENIChomozygous108559252
1227438054227438055GA29GENIChomozygous108999185
1227438802227438803A22GENIChomozygous127488206
1227435116227435117GA22GENIChomozygous120476064