chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4107882963107882964AT6GENIChomozygous126021755
4107947403107947404GA10GENIChomozygous126021756
4108122833108122834TC26GENIChomozygous126021757
4108351542108351543AG15GENICheterozygous126021758
4108407122108407123GT18GENIChomozygous126021759
4108456014108456015AT4GENIChomozygous126021760
4108512651108512652TA15GENIChomozygous126021761
4108512768108512769GA17GENIChomozygous126021762
4108515951108515952TA12GENIChomozygous126021763
4108515964108515965GT12GENIChomozygous126021764
4108515980108515981TG7GENIChomozygous126021765
4108516052108516053GC5GENIChomozygous126021766
4108516108108516109GT23GENIChomozygous126021767
4108550667108550668TG11GENIChomozygous126021768
4108559908108559909CA14GENIChomozygous126021769
4108559973108559974CG14GENIChomozygous126021770
4108560024108560025TC16GENIChomozygous126021771
4108560063108560064CT4GENIChomozygous126021772
4108647571108647572AG14GENICheterozygous112806692
4108647583108647584TA11GENICheterozygous112806694
4108653234108653235AG9GENICheterozygous126021773
4108653242108653243AG10GENICheterozygous126021774
4108653294108653295GT12GENICheterozygous126021775
4108653414108653415GC23GENICheterozygous126021776
4108653451108653452TG15GENICheterozygous126021777
4108685804108685805CT9GENIChomozygous126021778
4108697269108697270CA26GENIChomozygous112806720
4108762966108762967GT28GENICheterozygous126021779
4108818495108818496GC10GENIChomozygous112806738
4108884554108884555AG7GENICheterozygous126021780
4108918767108918768GT5GENICheterozygous126021781
4108980925108980926TC18GENIChomozygous112806772
4109021961109021962GC7GENICheterozygous126021782