chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147945967079459671CT80GENICpossibly homozygous114097770
147945970679459707AT76GENICpossibly homozygous114097771
147945970879459709TC73GENICpossibly homozygous113498839
147945981879459819TC57GENIChomozygous113498841
147946008079460081CT69GENIChomozygous113498842
147946051579460516GA60GENIChomozygous113498846
147946223179462232GA56GENIChomozygous114097772
147946371479463715GA55GENIChomozygous114097773
147946377179463772AG66GENIChomozygous113498854
147946424779464248AC65GENIChomozygous113498855