chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172478004172478005AG24GENIChomozygous114092611
5172479101172479102GA38GENIChomozygous119189100
5172480964172480965CG13GENIChomozygous119189101
5172481342172481343TC22GENIChomozygous114092613
5172481517172481518TC20GENIChomozygous114092615
5172483880172483881GA27GENIChomozygous119189102
5172484689172484690GA39GENIChomozygous119189103
5172485944172485945CT29GENIChomozygous119189104
5172486685172486686TC27GENIChomozygous114546126
5172487010172487011TC34GENIChomozygous114092619
5172487716172487717AG22GENIChomozygous114092621
5172488081172488082CT26GENIChomozygous119189105
5172488364172488365CA16GENIChomozygous119189106