chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71105449911054500TC11GENIChomozygous115567900
71105517111055172GA10GENIChomozygous115567901
71105612411056125CA22GENIChomozygous115567902
71105696611056967AG12GENIChomozygous115567903
71105893611058937AT18GENIChomozygous115567907
71105984711059848GC17GENIChomozygous115567908
71106024511060246TC22GENIChomozygous115567910
71106028911060290GA29GENIChomozygous115567911
71106029011060291CA29GENIChomozygous115567912
71106037111060372CA12GENIChomozygous115567913
71106103611061037AG15GENIChomozygous115567914
71106107211061073GA17GENIChomozygous115567915
71106123211061233GT7GENIChomozygous115567916
71106132411061325AG17GENIChomozygous115567917
71106918611069187CT12GENIChomozygous115567918
71107196711071968TG16GENIChomozygous115567919
71107263211072633TG8GENIChomozygous115567924
71107426111074262AG17GENIChomozygous115567925
71107494911074950TA11GENICpossibly homozygous115567926
71107510811075109GA31GENIChomozygous115567927