chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2251456558251456559GC16GENIChomozygous110384627
2251457041251457042GT23GENIChomozygous110384629
2251458748251458749CA11GENIChomozygous110384631
2251459062251459063GT9GENIChomozygous110384633
2251460754251460755GA22GENICpossibly homozygous110384637
2251461975251461976AG13GENIChomozygous110384639
2251465732251465733GA15GENICheterozygous110384643
2251466044251466045CT12GENIChomozygous110384653
2251467538251467539AG10GENIChomozygous110384657
2251468769251468770TC23GENIChomozygous110384662
2251470162251470163GA32GENIChomozygous110384666
2251470545251470546GA20GENIChomozygous110384668
2251471141251471142CT10GENIChomozygous110384672
2251471690251471691AG19GENIChomozygous110384674
2251472309251472310CA23GENIChomozygous110384676
2251473451251473452GT24GENIChomozygous110384678
2251473990251473991AG23GENIChomozygous110384680
2251474155251474156AG15GENIChomozygous110384682
2251474801251474802GA16GENIChomozygous110384684
2251475927251475928GT5GENICheterozygous110384686
2251476561251476562AG19GENIChomozygous110384688
2251476948251476949CT4GENIChomozygous110384694
2251478785251478786AG21GENIChomozygous110384696
2251479183251479184GA18GENIChomozygous120132154
2251480095251480096GA14GENIChomozygous110384698
2251480546251480547AG14GENIChomozygous110384702
2251481886251481887AG22GENIChomozygous110384706
2251483738251483739GA25GENIChomozygous110384710
2251483827251483828AG20GENIChomozygous111194615
2251484074251484075TC18GENIChomozygous110384712
2251484503251484504AG21GENICheterozygous110384714
2251484755251484756AG13GENIChomozygous110384716
2251483880251483881AC24GENICpossibly homozygous110852897