chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101495206514952066G8GENIChomozygous128790828
101495206914952088ACGCGCGCGCGCCGCGCGC8GENIChomozygous128790829
101495208914952090CG5GENIChomozygous123312985
101495209314952094CA6GENIChomozygous123312986
101495209514952097CC6GENIChomozygous128790830
101495209914952099G5GENIChomozygous128790831
101495210414952104G8GENIChomozygous128790832
101495211414952115CA7GENIChomozygous123312990
101495211714952118A7GENIChomozygous128790833
101495212014952121A7GENIChomozygous128790834
101495215514952156GA8GENIChomozygous116859901
101495217514952175C3GENIChomozygous128790835
101495220014952201A5GENIChomozygous128790836
101495221814952219C5GENIChomozygous128790837
101495223914952240C5GENIChomozygous128790838
101495229114952292T5GENIChomozygous128790840
101495247814952478G5GENIChomozygous128790842
101496536114965362CG5GENIChomozygous117074905
101496897914968980CA4GENIChomozygous116497158
101500884815008849G6GENIChomozygous128790858
101500885515008855GAA6GENIChomozygous128790859
101499213914992139A3GENIChomozygous130390734
101499359614993597AG15GENIChomozygous117982513
101502955415029555A19GENIChomozygous128790864
101502955615029557AG19GENIChomozygous116497328
101502956615029567AG22GENIChomozygous116497330
101502968615029687G26GENIChomozygous128790865
101502968815029689TC26GENIChomozygous123313045
101502969515029696T26GENIChomozygous128790866
101502969815029698G26GENIChomozygous128790867
101502970515029706T23GENIChomozygous128790868
101502970815029709TC23GENIChomozygous123313049