chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147501055147501056AG32GENIChomozygous114152811
5147501917147501918TC31GENIChomozygous114046100
5147502749147502750GA28GENIChomozygous114152812
5147502931147502932TC34GENIChomozygous114152813
5147502956147502957TC37GENIChomozygous114152814
5147506057147506058GA42GENIChomozygous114152816
5147506682147506683CT39GENIChomozygous114152817
5147507505147507506GT28GENIChomozygous114046110
5147508959147508960AG26GENIChomozygous114046118
5147509949147509950CT14GENIChomozygous114152820
5147511345147511346TC33GENIChomozygous114046122
5147514265147514266CT14GENIChomozygous114046124
5147514684147514685CT32GENIChomozygous118846519
5147514685147514686TC31GENIChomozygous118846521
5147515380147515381TC27GENIChomozygous118983215
5147515414147515415GA27GENIChomozygous118983216
5147525514147525515GA26GENIChomozygous114152826
5147530558147530559AC27GENIChomozygous114152827
5147530741147530742AG16GENIChomozygous114152828
5147531132147531133CT30GENIChomozygous114152829
5147531718147531719AT42GENIChomozygous114046154
5147531839147531840GT35GENIChomozygous114046156
5147531865147531866CT24GENIChomozygous114046158
5147534997147534998AG21GENIChomozygous114046162