chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141722898917228990AG19GENIChomozygous113361717
141722910017229101CT4GENIChomozygous113361719
141722930217229303AT4GENIChomozygous113361721
141723074717230748TC16GENIChomozygous113361723
141723115817231159TA12GENICheterozygous113361725
141723146017231461TC10GENIChomozygous113361727
141723161717231618TG8GENIChomozygous113361729
141723245817232459CT13GENIChomozygous113361731
141723250117232502TG13GENIChomozygous113361733
141723260117232602GA23GENIChomozygous113361735
141723282117232822TC10GENIChomozygous113361737
141723283017232831CT11GENIChomozygous113361739
141723369817233699GA17GENIChomozygous113361741
141722988117229882GC6GENICheterozygous125905870
141723212617232127AG3GENICheterozygous125945116
141723312517233126AT10GENICheterozygous125945117
141723313317233134GA7GENICheterozygous125945118