chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124046910140469103AA--15GENICheterozygous50543630
124046910240469103A-15GENICpossibly homozygous50563495
124047611140476112T-21GENIChomozygous50203611
124047621040476211CA19GENIChomozygous50203612
124047621140476212TC18GENIChomozygous50203613
124047652540476526AC26GENIChomozygous50203614
124048246540482466GGGGCA25GENIChomozygous50948327
124048266640482667AG30GENIChomozygous50948330
124048648340486484T-29GENIChomozygous50203621
124048648740486488TC33GENIChomozygous50203622
124048649040486491GT35GENIChomozygous50203623
124048651440486515TC29GENIChomozygous50203624
124048652540486526AT30GENIChomozygous50203625
124048654940486550GA41GENIChomozygous50203626
124048655340486554GT41GENIChomozygous50203627
124048658240486583TTG39GENIChomozygous50203628
124048658740486588A-38GENIChomozygous50203629
124048689340486894TTACAC13GENIChomozygous50571688
124048938740489388GA32GENIChomozygous50948333
124049091540490916TC30GENIChomozygous50203640
124049249240492493GA34GENIChomozygous50203641