chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2257490869257490870TC25GENIChomozygous111043696
2257492890257492891GA13GENIChomozygous111196876
2257493765257493766AG27GENIChomozygous111043698
2257494963257494964CT26GENIChomozygous111196878
2257495742257495743GA11GENIChomozygous110412029
2257495897257495898TC20GENIChomozygous110412031
2257496370257496371TC19GENIChomozygous111043700
2257497476257497477AC12GENIChomozygous111196880
2257498534257498535CT16GENIChomozygous111196882
2257501509257501510TC26GENIChomozygous111043706
2257507343257507344CA5GENIChomozygous110412060
2257507701257507702CG18GENIChomozygous111196892
2257510927257510928TC27GENIChomozygous111043724
2257512210257512211CA12GENIChomozygous111196898
2257513562257513563TC16GENIChomozygous111043742
2257516086257516087TC23GENIChomozygous110412076
2257517094257517095AG19GENIChomozygous110412078
2257517303257517304TG23GENIChomozygous110412080
2257517540257517541CT15GENIChomozygous110412082
2257518847257518848TC14GENIChomozygous110412084
2257519179257519180GA15GENIChomozygous110412086
2257519469257519470AG27GENIChomozygous110412088
2257522385257522386GA10GENICpossibly homozygous111196904
2257527018257527019TC21GENIChomozygous110412094
2257535895257535896GA8GENIChomozygous111196908
2257536476257536477CT9GENIChomozygous111196910
2257538232257538233AG11GENIChomozygous111196912
2257539607257539608GA27GENIChomozygous111196914
2257546308257546309GA16GENIChomozygous111196922
2257546589257546590GA14GENIChomozygous111196924