chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
389829848982985GA10GENIChomozygous111442594
389835598983560CT17GENIChomozygous111442595
389836258983626CG14GENIChomozygous111442596
389842678984268TA5GENIChomozygous111442597
389843058984306TA11GENIChomozygous111442598
389850278985028AG10GENIChomozygous111442599
389855888985589GA5GENICheterozygous125858812
389873468987347CG4GENIChomozygous111442603
389893458989346TC16GENIChomozygous111442611
389906338990634TC11GENIChomozygous111442612
389923788992379AG7GENIChomozygous111442613
389926378992638AG16GENIChomozygous111442614
389948468994847GA13GENIChomozygous111442615
389955958995596CA4GENICheterozygous125955384
389973408997341AG6GENIChomozygous111442616
389982298998230GA6GENIChomozygous111442617
389988578998858GA24GENIChomozygous120076870
390029759002976CT12GENIChomozygous111442619
390034199003420GA24GENIChomozygous111442620
390049659004966TG21GENIChomozygous111442621
390056899005690GA16GENIChomozygous111442622
390065329006533TC12GENIChomozygous111442623
390068469006847TC12GENIChomozygous111442624
390078889007889CT11GENIChomozygous111442625
390087439008744CT5GENICheterozygous111442626
390094699009470AG5GENIChomozygous111442627
390096289009629TC9GENIChomozygous111442628
390107119010712CT7GENIChomozygous111442629
390111229011123GA14GENIChomozygous111442630