chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107627869176278692GA17GENIChomozygous52257241
107627950176279502T-24GENIChomozygous51500487
107628038076280381CT19GENIChomozygous52257243
107628039976280400CG19GENIChomozygous51500488
107628076076280761AG21GENIChomozygous51500489
107628179076281791CT25GENIChomozygous52257244
107628274076282741TG24GENIChomozygous51500490
107628282676282827AG19GENIChomozygous52257246
107628338776283388A-10GENICheterozygous51697853
107628384076283841AG23GENIChomozygous51500492
107628388276283883TC25GENIChomozygous51500494
107628391176283912CCCCAAGCA27GENIChomozygous51500495
107628395376283954TC24GENIChomozygous51500497
107628397076283971CG23GENIChomozygous51500498
107628399676283997TC17GENIChomozygous52257248
107628478676284787CCCA11GENIChomozygous52257250
107628534676285347AG27GENIChomozygous52257252
107628684676286847CT30GENIChomozygous52257254
107628687176286872TC29GENIChomozygous52257256
107628757476287575T-3GENICheterozygous51500501
107628832776288328GGA15GENICpossibly homozygous52257260
107628922876289229CCT21GENIChomozygous51500504
107628947176289472CT24GENIChomozygous51500505
107628990676289907A-25GENICpossibly homozygous51697867
107629119876291199T-4GENIChomozygous51500506
107628886276288863GA22GENIChomozygous52257262
107629086776290870AAG---9GENIChomozygous52257264
107629096876290969CT15GENIChomozygous52257266