chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71107022711070228TC16GENIChomozygous53787298
71107044511070446TA17GENIChomozygous53787303
71107061011070611CT9GENIChomozygous53787304
71107073011070731GC16GENIChomozygous53787305
71107106511071066GA19GENIChomozygous53787307
71107136811071369AT17GENIChomozygous53787311
71107139511071396GA20GENIChomozygous53787312
71107190211071903TC18GENIChomozygous53787313
71107190611071907AG17GENIChomozygous53787314
71107204711072048AG15GENIChomozygous53787315
71107224511072246GA18GENIChomozygous53787316
71107239811072399AG19GENIChomozygous53787317
71107242811072429CG13GENIChomozygous53787318
71107242911072430AG13GENIChomozygous53787319
71107252511072526CT14GENIChomozygous53787320
71107271211072713GT5GENIChomozygous53787325
71107272811072729AC7GENIChomozygous53787327
71107305611073057GA10GENIChomozygous53787339
71107307011073071AAC9GENIChomozygous53787340
71107328511073286CT8GENIChomozygous53787343
71107330311073304AG11GENIChomozygous53787344
71107369011073691CT22GENICheterozygous53787352
71107370411073705CT21GENICheterozygous53787353
71107372311073724CG21GENICheterozygous53787354
71107375311073754TC17GENIChomozygous53787355
71107396711073968CT8GENIChomozygous53787357
71107430511074306GA7GENIChomozygous56472152