chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212695891212695892CT16GENIChomozygous108527182
1212695951212695952CT20GENIChomozygous108988782
1212695977212695978CT25GENIChomozygous108527184
1212696262212696263TA26GENIChomozygous108527188
1212697061212697062AT15GENIChomozygous108527190
1212697144212697145AG24GENIChomozygous108527192
1212697930212697931GA16GENICpossibly homozygous108988783
1212697990212697991CT21GENIChomozygous108988784
1212697991212697992CT21GENIChomozygous108988785
1212699581212699582TC27GENIChomozygous108527196
1212699650212699651CT25GENIChomozygous108988786
1212699774212699775GT23GENIChomozygous108988787
1212700052212700053AG18GENIChomozygous108527198
1212700320212700321GA7GENIChomozygous108988788
1212700453212700454TC12GENIChomozygous108527201
1212700622212700623GT20GENIChomozygous108527203
1212700644212700645CT21GENIChomozygous108988789
1212701080212701081GA12GENIChomozygous108988790
1212701790212701791TC19GENIChomozygous108527209
1212703093212703094GA27GENIChomozygous108527217
1212704986212704987TC9GENIChomozygous108527223
1212705157212705158AG15GENIChomozygous108527225
1212705313212705314AG23GENIChomozygous108527227
1212705337212705338AG26GENIChomozygous108527229
1212705357212705358AG27GENIChomozygous108527231
1212705400212705401CG21GENIChomozygous108527233
1212705626212705627AG11GENIChomozygous108527235
1212705841212705842AG16GENIChomozygous108527237
1212706018212706019AG25GENIChomozygous108527239
1212706202212706203TC25GENIChomozygous108527241
1212706376212706377CT21GENIChomozygous108527243
1212706413212706414GT18GENIChomozygous108527245
1212706416212706417TC17GENIChomozygous108527247
1212706582212706583CT20GENIChomozygous108527249
1212706904212706905TC27GENIChomozygous108527251