chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9116102728116102729AG23GENIChomozygous117648977
9116109856116109857GA26GENICheterozygous117433346
9116111053116111054GT12GENIChomozygous117433347
9116122686116122687CT23GENIChomozygous117433348
9116122690116122691CT24GENIChomozygous117433349
9116122718116122719GT23GENIChomozygous117433350
9116122721116122722AT21GENIChomozygous117433351
9116144258116144259AT47GENIChomozygous117433354
9116171666116171667AG61GENICheterozygous117433356
9116171673116171674CA67GENICheterozygous117433357
9116171772116171773AG164GENICheterozygous120297179
9116171779116171780CA183GENICheterozygous120297180
9116171825116171826AG237GENICheterozygous117834638
9116171832116171833CA239GENICheterozygous117834640
9116171937116171938GA183GENICheterozygous117433359
9116189612116189613CA39GENIChomozygous117648978
9116189620116189621CG41GENIChomozygous117648979
9116206727116206728CA14GENICpossibly homozygous117433362
9116210374116210375CG26GENIChomozygous117433363
9116214823116214824GA35GENICheterozygous117433365