chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227429473227429474GC44GENIChomozygous108559218
1227429643227429644AC61GENICpossibly homozygous108559219
1227430046227430047TC50GENIChomozygous108559220
1227430337227430338TC42GENIChomozygous108559221
1227430355227430356CT37GENIChomozygous108559222
1227430385227430386CT36GENIChomozygous108559223
1227430596227430597AG46GENIChomozygous108559224
1227430721227430722AG33GENIChomozygous108559225
1227430729227430730AG31GENIChomozygous108559226
1227430874227430875AG39GENIChomozygous108559227
1227431045227431046TC44GENIChomozygous108559228
1227431155227431155T38GENIChomozygous127488203
1227431973227431974TC33GENIChomozygous108559232
1227431460227431461CA48GENIChomozygous108559229
1227431634227431635TC42GENIChomozygous108559230
1227431795227431796AT36GENIChomozygous108559231
1227432241227432242TC55GENIChomozygous108559233
1227432281227432282GC49GENIChomozygous108559234
1227432968227432969GT43GENIChomozygous108559235
1227433338227433339CT37GENIChomozygous108559236
1227434140227434140A37GENIChomozygous127488205
1227434405227434406AG17GENIChomozygous108559237
1227434406227434407CG17GENIChomozygous108559238
1227434502227434503GA39GENIChomozygous108559239
1227435250227435251TC46GENIChomozygous108559241
1227436174227436175AG36GENIChomozygous108559243
1227437038227437039TC44GENIChomozygous108559244
1227437039227437040TG43GENIChomozygous108559245
1227437898227437899CG51GENICpossibly homozygous108559246
1227439268227439269AT42GENIChomozygous108559247
1227439444227439445TG49GENIChomozygous108559248
1227439680227439681CT28GENIChomozygous108559249
1227439916227439917TC45GENIChomozygous108559250
1227440363227440364CA46GENIChomozygous108559251
1227440669227440670TC51GENIChomozygous108559252
1227438054227438055GA51GENIChomozygous108999185
1227438802227438803A32GENIChomozygous127488206
1227435116227435117GA43GENIChomozygous120476064