chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84971036149710362AC18GENIChomozygous985602029
84971078749710788TG8GENIChomozygous985602030
84971137349711374AG14GENIChomozygous985602031
84971276549712766TC18GENIChomozygous985602032
84971277449712775TC18GENIChomozygous985602033
84971285849712859AG10GENIChomozygous985602034
84971408149714082AT14GENIChomozygous985602035
84971421149714212CT10GENIChomozygous985602036
84971462949714630AC13GENIChomozygous985602037
84971470249714703GA20GENIChomozygous985602038
84971524449715245AG8GENIChomozygous985602039
84971535249715353AG15GENIChomozygous985602040