chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134909454549094546GT25GENIChomozygous939103107
134909517449095175GC24GENIChomozygous939103108
134909540549095406AG14GENIChomozygous939103109
134909582549095826AC25GENIChomozygous939103110
134909638849096389GA30GENIChomozygous939103111
134909697349096974CT15GENIChomozygous939103112
134909725749097258GA24GENIChomozygous939103113
134909773249097733AG21GENIChomozygous939103114
134909813249098133CT28GENIChomozygous939103115
134909831249098313TC26GENIChomozygous939103116
134909915049099151GA16GENIChomozygous939103117
134909966849099669GC26GENIChomozygous939103118
134910029949100300CT27GENIChomozygous939103119
134910087549100876GA22GENIChomozygous939103120
134910158849101589GT26GENIChomozygous939103121
134910207849102079TC17GENIChomozygous939103122
134910254049102541CG18GENIChomozygous939103123
134910380649103807AG15GENIChomozygous939103124
134910413649104137CT33GENIChomozygous939103125
134910435649104357TC35GENIChomozygous939103126
134910500149105002AG19GENIChomozygous939103127
134910535849105359CT23GENIChomozygous939103128
134910771849107719AG7GENIChomozygous939103129
134910806349108064TC18GENIChomozygous939103130
134910817149108172AG23GENIChomozygous939103131
134910874949108750CT25GENIChomozygous939103132