chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83916815739168158CT11GENIChomozygous52589862
83916816239168163CT12GENIChomozygous52589863
83916903639169037CT10GENIChomozygous52589864
83916922539169226GA8GENIChomozygous52589865
83916959439169595AG17GENIChomozygous52589866
83916973539169736TG18GENIChomozygous52589867
83916974039169741GT16GENIChomozygous52589868
83917091239170913CT15GENIChomozygous52589870
83917120339171204GA16GENIChomozygous52961720
83917204239172045TTT---14GENIChomozygous52961722
83917244039172441GGA19GENICpossibly homozygous52961726