chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125207803752078038GA45GENIChomozygous50249102
125208068152080682AT35GENIChomozygous50249104
125208123952081240TTA17GENIChomozygous50249106
125208323552083236TC46GENIChomozygous50249108
125208353752083538CT42GENIChomozygous50249110
125208421152084212GGACACACAC28GENICheterozygous50547444
125208421252084220ACACACAC--------28GENICheterozygous50547445
125208421452084220ACACAC------28GENICpossibly homozygous50547446
125208478952084790AG36GENIChomozygous50249114
125208575052085751CG41GENIChomozygous50249116
125208592552085926TC44GENIChomozygous50249118
125208636352086364GC48GENIChomozygous50249120
125208673052086731GC50GENIChomozygous50249122
125208714952087150GA35GENIChomozygous50249124
125208807252088073C-34GENIChomozygous50249126
125208807952088080C-36GENIChomozygous50249128
125208808952088090GT40GENIChomozygous50249130
125208809652088097G-39GENIChomozygous50249132