chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1795520339552034CT14GENIChomozygous951048687
1795531469553147AG17GENICpossibly homozygous951048688
1795533899553390TC10GENIChomozygous951048689
1795540759554076TG12GENIChomozygous951048690
1795550049555005GT11GENIChomozygous951048691
1795550849555085TA9GENIChomozygous951048692
1795562369556237AG8GENIChomozygous951048693
1795565539556554CT15GENIChomozygous951048694
1795573989557399GA20GENIChomozygous951048695
1795574379557438CA16GENIChomozygous951048696
1795579559557956GA9GENIChomozygous951048697
1795579599557960GA11GENIChomozygous951048698
1795585769558577TC8GENIChomozygous951048699