chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212695891212695892CT28GENIChomozygous108527182
1212695977212695978CT28GENIChomozygous108527184
1212696163212696164GA31GENIChomozygous108527186
1212696262212696263TA33GENIChomozygous108527188
1212697061212697062AT23GENIChomozygous108527190
1212697144212697145AG33GENIChomozygous108527192
1212699295212699296GA29GENIChomozygous108527194
1212699581212699582TC25GENIChomozygous108527196
1212700052212700053AG22GENIChomozygous108527198
1212700082212700083CT21GENIChomozygous108527200
1212700453212700454TC25GENIChomozygous108527201
1212700622212700623GT21GENIChomozygous108527203
1212701123212701124GT27GENIChomozygous108527205
1212701272212701273AG30GENIChomozygous108527207
1212701790212701791TC20GENIChomozygous108527209
1212701830212701831CT22GENIChomozygous108527211
1212702144212702145CT14GENIChomozygous108527213
1212702564212702565CA24GENIChomozygous108527215
1212703093212703094GA25GENIChomozygous108527217
1212703362212703363TC22GENIChomozygous108527219
1212703529212703530CT13GENIChomozygous108527221
1212704986212704987TC33GENIChomozygous108527223
1212705157212705158AG33GENIChomozygous108527225
1212705313212705314AG23GENIChomozygous108527227
1212705337212705338AG24GENIChomozygous108527229
1212705357212705358AG25GENIChomozygous108527231
1212705400212705401CG24GENIChomozygous108527233
1212705626212705627AG28GENIChomozygous108527235
1212705841212705842AG35GENIChomozygous108527237
1212706018212706019AG30GENIChomozygous108527239
1212706202212706203TC28GENIChomozygous108527241
1212706376212706377CT23GENIChomozygous108527243
1212706413212706414GT23GENIChomozygous108527245
1212706416212706417TC24GENIChomozygous108527247
1212706582212706583CT32GENIChomozygous108527249
1212706904212706905TC18GENIChomozygous108527251