chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224700530224700531TC30GENIChomozygous57111750
4224701433224701434CA26GENIChomozygous57111752
4224701718224701719A-3GENIChomozygous57111754
4224702711224702718CATCAAT-------19GENICheterozygous57648182
4224702723224702724AG21GENICheterozygous57111758
4224702849224702855ACACAC------11GENIChomozygous57111762
4224703930224703931CG36GENIChomozygous57111764
4224705662224705663CT32GENIChomozygous57111766
4224702730224702731CT24GENICheterozygous57368965
4224707563224707564AG46GENIChomozygous57111768
4224707982224707983CT46GENIChomozygous57111770
4224714424224714425TTA30GENICpossibly homozygous57111774
4224716944224716952TATGTATG--------1GENIChomozygous57111776
4224720265224720266AAG25GENIChomozygous57111778
4224720267224720268GGA19GENIChomozygous57111782
4224721495224721496CCT7GENICheterozygous57368969
4224721496224721497T-7GENICheterozygous57368971
4224713505224713506CT30GENICheterozygous57760879