chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
179625970096259701TC16GENIChomozygous64791687
179625989396259894CA12GENIChomozygous64791691
179626071396260714GA16GENIChomozygous64981215
179626256396262564TC14GENIChomozygous64662760
179626501196265012AG9GENIChomozygous64662763
179627099496270995AC10GENIChomozygous64791699
179627249096272491TG3GENIChomozygous64662772
179627499596274996AG12GENIChomozygous64662775
179627755996277560CT3GENIChomozygous64981216
179627886496278865TC17GENIChomozygous64791705
179628063896280639TC18GENIChomozygous64662778
179628205296282053CG2GENIChomozygous64791711
179628233096282331GA12GENIChomozygous64981217
179628233496282335AG13GENIChomozygous64896555
179628258896282589AG12GENIChomozygous64981218
179628461496284615CT8GENIChomozygous64981219
179628577096285771CT20GENIChomozygous64981220
179628875496288755CT23GENIChomozygous64981221
179629226296292263TC14GENIChomozygous64981222
179629416896294169AG6GENIChomozygous64662789
179629423596294236CT9GENIChomozygous64981223
179629461696294617TA7GENIChomozygous64981224
179629834496298345AG4GENIChomozygous64791737
179630964096309641TG6GENIChomozygous64981225
179631581396315814GA7GENIChomozygous64981226
179632172096321721GA6GENIChomozygous64981227
179628206496282065CG5GENIChomozygous65613655
179630260996302610CT5GENICheterozygous65050293