chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2054084665408467TG23GENIChomozygous45731733
2054085095408510AG15GENIChomozygous45386657
2054086245408625T-12GENIChomozygous45731734
2054089515408952AT32GENIChomozygous45731735
2054096575409658CT29GENIChomozygous45731736
2054102095410210GA28GENIChomozygous45731737
2054103495410350AACGAGG28GENIChomozygous45386665
2054105235410524TC13GENICpossibly homozygous45386667
2054116385411639A-1GENIChomozygous45386673
2054121715412172TA22GENIChomozygous45731738
2054121945412195TC21GENIChomozygous45731739
2054122165412244ATATATATATAAATAAATAAATAAATAA----------------------------9GENIChomozygous45386681
2054125945412595AAAAAC16GENIChomozygous45386688
2054126535412654GA24GENIChomozygous45386690
2054128985412899AT25GENICheterozygous45731740
2054129295412930TC31GENICheterozygous45731741
2054129305412931AG30GENICheterozygous45731742
2054129315412932GC31GENICheterozygous45731743
2054132095413210GA21GENIChomozygous45731744
2054132535413254AC17GENIChomozygous45731745
2054133245413325CT12GENIChomozygous45731746
2054134195413420GA12GENIChomozygous45731747
2054137405413741CA29GENIChomozygous45386709
2054146245414625GC29GENIChomozygous45386720
2054146865414687GC37GENIChomozygous45386722
2054147335414735GC--32GENICpossibly homozygous45386724
2054147355414736GT33GENICheterozygous45386726
2054147375414740GGC---32GENICpossibly homozygous45386728
2054148155414816CT30GENIChomozygous45731748
2054148235414824GA31GENIChomozygous45731749
2054149175414920ACG---29GENIChomozygous45386730
2054150045415007GTC---19GENIChomozygous45386732
2054150135415015GT--25GENICheterozygous45386734
2054150165415017G-25GENICheterozygous45386736
2054152225415223TC24GENIChomozygous45386738
2054155085415509TC37GENIChomozygous45386740
2054166455416646CT13GENIChomozygous45731750
2054193265419327CG40GENICheterozygous45386750