chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145374787145374788CA17GENIChomozygous114038655
5145374863145374864GA15GENIChomozygous114038656
5145374895145374896CT12GENIChomozygous114038657
5145374916145374917GA16GENIChomozygous114038658
5145375065145375066TC18GENIChomozygous114038659
5145375143145375144TC12GENIChomozygous114038660
5145375152145375153T12GENIChomozygous128250682
5145375168145375169TC11GENIChomozygous114038661
5145375322145375323AG15GENIChomozygous114038662
5145375763145375764GT18GENIChomozygous114038663
5145376042145376043TC18GENIChomozygous114038664
5145376262145376263AG10GENIChomozygous114345835
5145376636145376636GT15GENIChomozygous128250683
5145377095145377096AG11GENIChomozygous114038665
5145377112145377113GA10GENIChomozygous114038666
5145377176145377177GA11GENIChomozygous114038667