chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227429473227429474GC19GENIChomozygous108559218
1227429643227429644AC29GENIChomozygous108559219
1227430046227430047TC18GENIChomozygous108559220
1227430337227430338TC13GENIChomozygous108559221
1227430355227430356CT15GENIChomozygous108559222
1227430385227430386CT17GENIChomozygous108559223
1227430596227430597AG20GENIChomozygous108559224
1227430721227430722AG24GENIChomozygous108559225
1227430729227430730AG27GENIChomozygous108559226
1227430874227430875AG25GENIChomozygous108559227
1227431045227431046TC25GENIChomozygous108559228
1227431460227431461CA33GENIChomozygous108559229
1227431634227431635TC23GENIChomozygous108559230
1227431795227431796AT19GENIChomozygous108559231
1227431973227431974TC14GENIChomozygous108559232
1227432241227432242TC28GENIChomozygous108559233
1227432281227432282GC29GENIChomozygous108559234
1227432968227432969GT28GENIChomozygous108559235
1227433338227433339CT30GENICpossibly homozygous108559236
1227434405227434406AG18GENIChomozygous108559237
1227434406227434407CG18GENIChomozygous108559238
1227434502227434503GA19GENIChomozygous108559239
1227435250227435251TC28GENIChomozygous108559241
1227436174227436175AG17GENIChomozygous108559243
1227437038227437039TC12GENIChomozygous108559244
1227437039227437040TG12GENIChomozygous108559245
1227437898227437899CG19GENIChomozygous108559246
1227439268227439269AT23GENIChomozygous108559247
1227439444227439445TG20GENIChomozygous108559248
1227439680227439681CT26GENIChomozygous108559249
1227439916227439917TC21GENIChomozygous108559250
1227440363227440364CA25GENIChomozygous108559251
1227440669227440670TC31GENIChomozygous108559252
1227438054227438055GA11GENIChomozygous108999185
1227435112227435113GA38GENICheterozygous108999184