chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221645792221645793TC29GENIChomozygous108544940
1221646358221646359TC25GENIChomozygous108544942
1221646397221646398CT19GENIChomozygous108544945
1221646665221646666CT30GENIChomozygous108544947
1221648005221648006GA9GENIChomozygous108544949
1221648240221648241CT12GENIChomozygous108544951
1221649722221649723CT18GENIChomozygous108544953
1221650642221650643GC16GENIChomozygous108544959
1221650707221650708TC21GENIChomozygous108544961
1221651452221651453TC28GENIChomozygous108544963
1221652245221652246CA18GENIChomozygous108544965
1221653162221653163CA20GENIChomozygous108544967
1221653197221653198AG23GENIChomozygous108544969
1221654338221654339AG28GENIChomozygous108544971
1221656164221656165GA22GENIChomozygous108544973
1221657029221657030CT22GENIChomozygous108544975
1221657896221657897AG14GENIChomozygous108544977
1221658711221658712TC9GENIChomozygous108544979
1221659252221659253CT14GENIChomozygous108544981
1221659909221659910CT26GENIChomozygous108544983
1221660381221660382GC15GENIChomozygous108544985
1221661142221661143TC27GENIChomozygous108544987
1221661306221661307GA28GENIChomozygous108544989
1221661745221661746TC19GENIChomozygous108544991
1221662025221662026TG23GENIChomozygous108544993
1221662902221662903GA18GENIChomozygous108544995
1221663730221663731TC7GENIChomozygous108544997
1221666736221666737TG6GENIChomozygous108544999
1221666756221666757AG9GENIChomozygous108545001