chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6144188094144188095AC13GENIChomozygous54762006
6144188672144188673CT27GENICpossibly homozygous54762007
6144189314144189315AG21GENIChomozygous54762008
6144189654144189655CT24GENICheterozygous54762009
6144190175144190176CT4GENIChomozygous54762010
6144190536144190537AG29GENICpossibly homozygous54762012
6144190745144190746TC11GENIChomozygous55439531
6144190746144190747AT10GENIChomozygous55439533