chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212232675212232676AG43GENIChomozygous806071035
1212246839212246840TC50GENICpossibly homozygous806071036
1212246883212246884GT63GENIChomozygous806071037
1212246939212246940CG64GENICpossibly homozygous806071038
1212252432212252433TG49GENIChomozygous806071039
1212262916212262917AC23GENICpossibly homozygous806071040
1212262936212262937TG23GENIChomozygous806071041
1212263032212263033TG13GENIChomozygous806071042
1212263077212263078AC18GENIChomozygous806071043
1212263129212263130AG17GENIChomozygous806071044
1212264037212264038GT36GENIChomozygous806071045
1212264187212264188AC42GENIChomozygous806071046
1212274307212274308GT43GENIChomozygous806071047
1212275738212275739AC36GENIChomozygous806071048
1212275844212275845CA38GENIChomozygous806071049
1212276381212276382CT47GENICpossibly homozygous806071050