chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221645792221645793TC38GENIChomozygous108544940
1221646358221646359TC56GENIChomozygous108544942
1221646397221646398CT40GENIChomozygous108544945
1221646665221646666CT39GENIChomozygous108544947
1221648005221648006GA48GENIChomozygous108544949
1221648240221648241CT31GENIChomozygous108544951
1221649722221649723CT36GENIChomozygous108544953
1221650707221650708TC40GENIChomozygous108544961
1221651452221651453TC29GENIChomozygous108544963
1221652245221652246CA30GENIChomozygous108544965
1221653162221653163CA49GENIChomozygous108544967
1221653197221653198AG53GENIChomozygous108544969
1221654338221654339AG52GENIChomozygous108544971
1221656164221656165GA35GENIChomozygous108544973
1221657896221657897AG61GENIChomozygous108544977
1221659252221659253CT48GENIChomozygous108544981
1221659909221659910CT39GENIChomozygous108544983
1221660381221660382GC38GENIChomozygous108544985
1221661142221661143TC33GENIChomozygous108544987
1221661306221661307GA42GENIChomozygous108544989
1221661745221661746TC50GENIChomozygous108544991
1221662025221662026TG51GENIChomozygous108544993
1221662902221662903GA47GENIChomozygous108544995
1221663730221663731TC42GENIChomozygous108544997
1221666736221666737TG41GENIChomozygous108544999
1221666756221666757AG48GENICpossibly homozygous108545001