chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186061949260619493AG59GENIChomozygous782937287
186061975460619755GT22GENICheterozygous782937288
186062046560620466TC49GENIChomozygous782937289
186062056060620561GT70GENIChomozygous782937290
186062060360620604TC58GENIChomozygous782937291
186062106960621070GA63GENIChomozygous782937292
186062138360621384TA71GENIChomozygous782937293
186062138760621388AG70GENIChomozygous782937294
186062282960622830TC54GENIChomozygous782937295
186062320460623205CA43GENIChomozygous782937296
186062329660623297TC43GENICheterozygous782937297
186062330560623306CT43GENICheterozygous782937298
186062580060625801TC55GENIChomozygous782937299
186062663260626633TC73GENIChomozygous782937300
186062748460627485TC47GENIChomozygous782937301
186062846460628465AC49GENIChomozygous782937302
186062880060628801AG78GENIChomozygous782937303