chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147501917147501918TC33GENIChomozygous114046100
5147502749147502750GA23GENIChomozygous114152812
5147502931147502932TC17GENIChomozygous114152813
5147502956147502957TC19GENIChomozygous114152814
5147506057147506058GA34GENIChomozygous114152816
5147506682147506683CT44GENIChomozygous114152817
5147507505147507506GT22GENIChomozygous114046110
5147511345147511346TC20GENIChomozygous114046122
5147514684147514685CT42GENIChomozygous118846519
5147514685147514686TC42GENIChomozygous118846521
5147523930147523931AG10GENIChomozygous114046132
5147523954147523955AG14GENIChomozygous114046134
5147525514147525515GA21GENIChomozygous114152826
5147527409147527410AG2GENIChomozygous114046150
5147530558147530559AC33GENIChomozygous114152827
5147530741147530742AG12GENIChomozygous114152828
5147531132147531133CT28GENIChomozygous114152829
5147531839147531840GT34GENIChomozygous114046156
5147534997147534998AG4GENIChomozygous114046162