chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212695891212695892CT29GENIChomozygous108527182
1212695977212695978CT20GENIChomozygous108527184
1212696163212696164GA17GENIChomozygous108527186
1212696262212696263TA20GENIChomozygous108527188
1212697061212697062AT28GENIChomozygous108527190
1212697144212697145AG32GENIChomozygous108527192
1212699295212699296GA21GENIChomozygous108527194
1212699581212699582TC23GENIChomozygous108527196
1212700052212700053AG8GENIChomozygous108527198
1212700082212700083CT17GENIChomozygous108527200
1212700453212700454TC19GENIChomozygous108527201
1212700622212700623GT22GENIChomozygous108527203
1212701123212701124GT23GENIChomozygous108527205
1212701272212701273AG23GENIChomozygous108527207
1212701790212701791TC21GENIChomozygous108527209
1212701830212701831CT24GENIChomozygous108527211
1212702144212702145CT22GENIChomozygous108527213
1212702564212702565CA11GENIChomozygous108527215
1212703093212703094GA9GENIChomozygous108527217
1212703362212703363TC17GENIChomozygous108527219
1212703529212703530CT18GENIChomozygous108527221
1212704986212704987TC16GENIChomozygous108527223
1212705157212705158AG10GENIChomozygous108527225
1212705313212705314AG24GENIChomozygous108527227
1212705337212705338AG12GENIChomozygous108527229
1212705357212705358AG14GENIChomozygous108527231
1212705400212705401CG22GENIChomozygous108527233
1212705626212705627AG22GENIChomozygous108527235
1212705841212705842AG18GENIChomozygous108527237
1212706018212706019AG25GENIChomozygous108527239
1212706202212706203TC25GENIChomozygous108527241
1212706376212706377CT20GENIChomozygous108527243
1212706413212706414GT4GENIChomozygous108527245
1212706416212706417TC7GENIChomozygous108527247
1212706582212706583CT24GENIChomozygous108527249
1212706904212706905TC28GENIChomozygous108527251