chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2181829893181829894TC9GENIChomozygous110157554
2181829975181829976GT10GENIChomozygous110157555
2181834497181834498AC15GENIChomozygous110157558
2181834594181834595TG11GENIChomozygous110157559
2181834947181834948GA8GENIChomozygous110157560
2181835029181835030GA24GENIChomozygous110157561
2181835925181835926TC24GENIChomozygous110157562
2181836049181836050AG10GENIChomozygous110157563
2181836959181836960TC20GENIChomozygous110157564
2181836990181836991CT18GENIChomozygous110157565
2181837190181837191TC19GENIChomozygous110157566
2181837655181837656TA13GENIChomozygous120376925
2181839098181839099GA11GENIChomozygous120376926
2181840439181840440AG32GENIChomozygous120376927
2181841703181841704TA19GENIChomozygous120376928
2181841739181841740AC17GENIChomozygous120376929
2181841971181841972AC19GENICpossibly homozygous110157568
2181843140181843141CG5GENIChomozygous120212496
2181844693181844694AC24GENIChomozygous120376930
2181846766181846767CT8GENIChomozygous110157570
2181848661181848662GA10GENIChomozygous110157571
2181853182181853183GA11GENIChomozygous120376931
2181853811181853812GA21GENIChomozygous120376932
2181854647181854648GA23GENIChomozygous110157572
2181855038181855039TC23GENIChomozygous120376933
2181855398181855399GT15GENIChomozygous120376934
2181855947181855948GA14GENIChomozygous120376935
2181862497181862498CT16GENIChomozygous120376936
2181864176181864177GT16GENIChomozygous110157576
2181864272181864273CA14GENIChomozygous120376937
2181865137181865138GC10GENIChomozygous110157577
2181865488181865489TA13GENIChomozygous110157578
2181868861181868862CT13GENIChomozygous120376938
2181869168181869169GA17GENIChomozygous110157580
2181869476181869477GA21GENIChomozygous120376939
2181870296181870297CT20GENIChomozygous120376941
2181870376181870377CT20GENIChomozygous120376942
2181870759181870760AC9GENICheterozygous111340964