chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1213636331213636332GA18GENIChomozygous108531690
1213636455213636456TG19GENIChomozygous108531691
1213637395213637396CT15GENIChomozygous108531692
1213637710213637711AG22GENIChomozygous108531693
1213638044213638045GA29GENIChomozygous108531694
1213638178213638179GA12GENIChomozygous108531695
1213638278213638279GA18GENIChomozygous108531696
1213638871213638872AG11GENIChomozygous125308300
1213639318213639319GT21GENIChomozygous108531697
1213640364213640365GA21GENIChomozygous108531698
1213641459213641460TC17GENIChomozygous108531699
1213641721213641722CA20GENIChomozygous108531700
1213642586213642587TC21GENIChomozygous108531701
1213646479213646480AT14GENIChomozygous108531702
1213647986213647987CT29GENIChomozygous108531703