chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124046910040469103AAA---8GENICheterozygous50558979
124046910240469103A-8GENICpossibly homozygous50563495
124047611140476112T-19GENIChomozygous50203611
124047621040476211CA21GENIChomozygous50203612
124047621140476212TC21GENIChomozygous50203613
124047652540476526AC15GENIChomozygous50203614
124048246540482466GGGGCA17GENIChomozygous50948327
124048266640482667AG26GENIChomozygous50948330
124048648340486484T-22GENIChomozygous50203621
124048648740486488TC22GENIChomozygous50203622
124048649040486491GT19GENIChomozygous50203623
124048651440486515TC18GENIChomozygous50203624
124048652540486526AT16GENIChomozygous50203625
124048654940486550GA25GENIChomozygous50203626
124048655340486554GT26GENIChomozygous50203627
124048658240486583TTG16GENIChomozygous50203628
124048658740486588A-16GENIChomozygous50203629
124048689340486894TTACAC2GENIChomozygous50571688
124048938740489388GA22GENIChomozygous50948333
124049091540490916TC22GENIChomozygous50203640
124049249240492493GA14GENIChomozygous50203641