chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124046910240469103A-12GENICheterozygous50563495
124047611140476112T-36GENIChomozygous50203611
124047621040476211CA33GENIChomozygous50203612
124047621140476212TC33GENIChomozygous50203613
124048648340486484T-33GENIChomozygous50203621
124048648740486488TC35GENIChomozygous50203622
124048649040486491GT36GENIChomozygous50203623
124048651440486515TC33GENIChomozygous50203624
124048652540486526AT36GENIChomozygous50203625
124048654940486550GA34GENIChomozygous50203626
124048655340486554GT32GENIChomozygous50203627
124048658240486583TTG27GENIChomozygous50203628
124048658740486588A-29GENIChomozygous50203629
124048690040486904ACAC----2GENICheterozygous50543636
124048690240486904AC--2GENICheterozygous50610458
124049446340494471ACACACAC--------4GENICheterozygous50571690