chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3124897238124897239CT20GENIChomozygous57651935
3124899509124899511TT--14GENICheterozygous57651937
3124899510124899511T-14GENICheterozygous57651938
3124899671124899675TATA----6GENIChomozygous57651940
3124899898124899899CT53GENIChomozygous57651942
3124904475124904476GA35GENIChomozygous57651944
3124907760124907761AG33GENIChomozygous57651946
3124910580124910581TC38GENIChomozygous57651948
3124910986124910987T-17GENICpossibly homozygous57651950
3124910991124910992TTTTA17GENICheterozygous57651952
3124910993124910994TTA17GENICheterozygous57651954
3124910995124910996AAT14GENIChomozygous57651956
3124911055124911056GA38GENICheterozygous57651958
3124912454124912455GA40GENIChomozygous57651960
3124915644124915645AG65GENICpossibly homozygous57651962
3124916557124916558TC56GENIChomozygous57651964
3124918967124918968TC32GENICheterozygous57651966
3124919431124919432AG28GENIChomozygous57651968
3124920654124920655GA37GENIChomozygous57651970
3124922179124922180TA36GENIChomozygous57651972
3124923390124923412TGTGTGTGTGTGTGTGTGTGTG----------------------6GENICheterozygous57651974
3124924691124924692CG17GENICheterozygous57651976
3124926081124926082AG25GENIChomozygous57651978
3124930190124930191TC51GENICheterozygous57651980
3124933626124933627GGAC4GENIChomozygous57651982