chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212232675212232676AG57GENIChomozygous778736810
1212246839212246840TC42GENIChomozygous778736811
1212246883212246884GT45GENIChomozygous778736812
1212246939212246940CG66GENICpossibly homozygous778736813
1212252432212252433TG66GENIChomozygous778736814
1212262916212262917AC29GENIChomozygous778736815
1212262936212262937TG19GENIChomozygous778736816
1212263032212263033TG8GENIChomozygous778736817
1212263077212263078AC29GENIChomozygous778736818
1212263129212263130AG34GENIChomozygous778736819
1212264037212264038GT60GENIChomozygous778736820
1212264187212264188AC51GENIChomozygous778736821
1212274307212274308GT47GENICpossibly homozygous778736822
1212275738212275739AC34GENIChomozygous778736823
1212275844212275845CA48GENICpossibly homozygous778736824
1212276381212276382CT50GENIChomozygous778736825