chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122431789024317891AG29GENIChomozygous115287674
122431910524319106TG34GENIChomozygous115287676
122431910624319107TC33GENIChomozygous115287678
122432094824320949TC25GENIChomozygous115287680
122432108124321082CG22GENIChomozygous115287682
122432108224321083CA22GENIChomozygous115287684
122432144624321447GA34GENIChomozygous115287686
122432204624322047AG38GENIChomozygous115287688
122432217524322176AC12GENIChomozygous115287690
122432264724322648TC22GENIChomozygous115287692
122432470224324703CT20GENIChomozygous115287694
122432538324325384AT28GENIChomozygous115287696
122432579424325795AC33GENIChomozygous115287698
122432666724326668TC28GENIChomozygous115287702
122432698224326983CT32GENIChomozygous115287704
122432810024328101CG34GENIChomozygous115287706
122432892224328923TC32GENIChomozygous115287708
122432911224329113AG25GENIChomozygous115287710
122433129324331294GT26GENIChomozygous115287714
122433213724332138TC37GENIChomozygous115287716
122433586824335869CT32GENIChomozygous115287718
122433615024336151GA38GENIChomozygous115422198
122433618024336181CT44GENIChomozygous115422200
122433686424336865TC39GENIChomozygous115287720
122433752224337523CA21GENIChomozygous115287722
122433933124339332GA47GENICheterozygous115485016
122433934124339342TC34GENICheterozygous115422202