chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1162741012162741013TC32GENIChomozygous108345798
1162742509162742510CT34GENIChomozygous108345802
1162743102162743103CT19GENIChomozygous108345804
1162743140162743141CT14GENIChomozygous108345806
1162743541162743542GA15GENIChomozygous108952044
1162746434162746435GC24GENIChomozygous108345815
1162746643162746644AG27GENIChomozygous108345821
1162747752162747753GA37GENIChomozygous108345823
1162747848162747849CT29GENIChomozygous108345825
1162748554162748555CG23GENIChomozygous108345827
1162748564162748565TC25GENIChomozygous108345829
1162749901162749902CA29GENIChomozygous108345837
1162750559162750560AC22GENIChomozygous108345839
1162751365162751366TA27GENIChomozygous120487110
1162753363162753364CT26GENIChomozygous108952049
1162753398162753399TC32GENIChomozygous108345843
1162753594162753595AC27GENIChomozygous108345845
1162753748162753749AC30GENIChomozygous108345849
1162760943162760944CA29GENIChomozygous108345861
1162761152162761153AG24GENIChomozygous108345865
1162761190162761191TG24GENIChomozygous108345867
1162762160162762161CG27GENIChomozygous108345869
1162764130162764131CT37GENIChomozygous108952057
1162764675162764676CT28GENIChomozygous108345873
1162764783162764784TG29GENIChomozygous108345875
1162765291162765292CT33GENIChomozygous108345879
1162766141162766142AG26GENIChomozygous108345883