chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142512954142512955TC18GENIChomozygous54268747
7142512985142512986AG16GENIChomozygous54161235
7142513253142513254G-16GENIChomozygous54161237
7142513334142513335AG17GENIChomozygous54161238
7142514694142514695TG35GENIChomozygous54161241
7142515006142515007AAGT13GENICpossibly homozygous54161242
7142515276142515277GGA13GENIChomozygous54268750
7142515779142515780GA33GENIChomozygous54161243
7142516071142516072AG38GENIChomozygous54161244
7142516326142516327TC25GENIChomozygous54161245