chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
520451602045161T-25GENIChomozygous56113190
520452262045227AG31GENIChomozygous56113192
520452942045295GC37GENIChomozygous56113193
520454612045462TC34GENIChomozygous56113195
520458222045823GC30GENIChomozygous56113197
520465742046575GGA22GENICpossibly homozygous56113199
520486752048676CCT23GENIChomozygous56113201
520493592049360AG37GENIChomozygous55184667
520503392050340GA29GENIChomozygous55184669
520505082050513AAAAG-----16GENICheterozygous56113203
520508642050866AA--11GENICheterozygous55184675
520508652050866A-11GENICheterozygous55184677
520527172052718GA24GENIChomozygous56113205
520537222053723GA41GENIChomozygous56113207
520537482053749TA46GENIChomozygous56113209
520537542053755CA45GENIChomozygous56113210
520537792053780GA44GENIChomozygous56113212
520538222053823GA43GENIChomozygous56113214
520538542053855GA31GENIChomozygous56113216
520538612053862GA30GENIChomozygous56113218
520538962053897GA34GENIChomozygous55184679
520546832054684CT26GENIChomozygous56113220
520551202055121GA35GENIChomozygous56113222
520551482055149AG30GENIChomozygous56113223
520562432056244AAACAC4GENIChomozygous56390393
520567252056726GA32GENIChomozygous56113227
520571162057117AG46GENIChomozygous56113229
520578662057867TTAA25GENICpossibly homozygous56113231
520594392059440TC32GENIChomozygous56113233