chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98179749681797497AC12GENICpossibly homozygous671509831
98179848381798484GT14GENICpossibly homozygous671509832
98179909681799097TA5GENIChomozygous671509833
98179917781799178TC6GENIChomozygous671509834
98179918181799182GT9GENICpossibly homozygous671509835
98180029281800293GA2GENIChomozygous671509836
98180061281800613TC21GENICpossibly homozygous671509837
98180086081800861GT17GENICpossibly homozygous671509838
98180152081801521CT9GENICheterozygous671509839
98180202381802024AG13GENIChomozygous671509840
98180369281803693TG8GENIChomozygous671509841
98180384781803848CT14GENIChomozygous671509842
98180426981804270AG4GENIChomozygous671509843
98180456281804563AG21GENICpossibly homozygous671509844
98180519581805196CT16GENIChomozygous671509845
98180587981805880AT8GENICpossibly homozygous671509846
98180598381805984AATCGTTCTTCTTCTAATGTCCTCCTTG2GENIChomozygous769057910
98180604781806048TG17GENICheterozygous671509847
98180723281807233TG13GENICheterozygous671509848
98180835281808353CCTTCCTTCCTTCA1GENIChomozygous769057911