chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
520451602045161T-20GENIChomozygous56113190
520452262045227AG18GENIChomozygous56113192
520452942045295GC25GENIChomozygous56113193
520454612045462TC21GENIChomozygous56113195
520458222045823GC31GENIChomozygous56113197
520465742046575GGA25GENICpossibly homozygous56113199
520486752048676CCT17GENICpossibly homozygous56113201
520493592049360AG12GENIChomozygous55184667
520503392050340GA23GENIChomozygous55184669
520504952050496TTAA11GENICheterozygous55184671
520505082050513AAAAG-----13GENIChomozygous56113203
520508642050866AA--8GENICheterozygous55184675
520508652050866A-8GENICheterozygous55184677
520527172052718GA27GENIChomozygous56113205
520537222053723GA34GENIChomozygous56113207
520537482053749TA31GENIChomozygous56113209
520537542053755CA30GENIChomozygous56113210
520537792053780GA33GENIChomozygous56113212
520538222053823GA23GENIChomozygous56113214
520538542053855GA18GENIChomozygous56113216
520538612053862GA19GENIChomozygous56113218
520538962053897GA17GENIChomozygous55184679
520546832054684CT26GENIChomozygous56113220
520551202055121GA24GENIChomozygous56113222
520551482055149AG26GENIChomozygous56113223
520562662056267TA10GENICheterozygous56113225
520562932056294CCT11GENICheterozygous56199655
520567252056726GA22GENIChomozygous56113227
520571162057117AG21GENIChomozygous56113229
520578662057867TTAA12GENIChomozygous56113231
520587902058791CT35GENICheterozygous55184689
520587982058799CT36GENICheterozygous55184691
520588142058815AG37GENICheterozygous55184693
520588332058834TC39GENICheterozygous55184695
520594392059440TC18GENIChomozygous56113233