chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154110103741101038CT19GENIChomozygous813910017
154110104241101043AC15GENIChomozygous813910018
154110104341101044AT15GENIChomozygous813910019
154110111741101118GC21GENICpossibly homozygous813910020
154110119341101194GC22GENIChomozygous813910021
154110120441101205CG24GENICpossibly homozygous813910022
154110277641102777CG34GENICheterozygous813910023
154110283541102836TC34GENICheterozygous813910024
154112372641123727GA32GENICheterozygous813910025
154117230641172307GT11GENIChomozygous813910026
154117250441172505CT20GENIChomozygous813910027