chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141371726141371727GA12GENIChomozygous115939944
7141372690141372691GT15GENIChomozygous118515687
7141373020141373021CA22GENIChomozygous118515688
7141373520141373521TC39GENIChomozygous115939945
7141374136141374137CT23GENIChomozygous118515689
7141374157141374158AG20GENIChomozygous115939947
7141374172141374173AC16GENIChomozygous118515690
7141374210141374211CA12GENIChomozygous118515691
7141375195141375196CG9GENIChomozygous115939950
7141375332141375333GA17GENICpossibly homozygous118515692