chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214053991214053992T-17GENICheterozygous61079523
1214064204214064205A-24GENIChomozygous61079538
1214064207214064208A-24GENIChomozygous61079539
1214064337214064338G-23GENIChomozygous61079540
1214064352214064353GA22GENIChomozygous61318958
1214064354214064355CG22GENIChomozygous61318959
1214064356214064357GC22GENIChomozygous61318960
1214064365214064366C-21GENIChomozygous61079541
1214065830214065831T-12GENICheterozygous62470431
1214077761214077762A-8GENICheterozygous62275577
1214089791214089792TTG8GENICheterozygous62485238
1214104186214104187AAT34GENIChomozygous61079607
1214104190214104191GGT31GENIChomozygous61079608
1214104201214104202AAT31GENIChomozygous61079609
1214104204214104205GGCTC30GENIChomozygous61079610
1214104399214104402CTC---22GENIChomozygous61079611
1214107006214107007TTC18GENIChomozygous61079617