chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103888927038889273AGC8GENICheterozygous69805295
103888927438889275GA3GENIChomozygous69805296
103888965038889651CT16GENIChomozygous68627063
103888979138889792AG10GENIChomozygous68358751
103889018638890187AC4GENIChomozygous68358753
103889022838890229CG12GENIChomozygous68358755
103889033238890333CA15GENIChomozygous68358757
103889067938890680TC10GENIChomozygous68358761
103889076238890762TTTA12GENICheterozygous69805297
103889083438890835TC14GENIChomozygous68358763
103889092638890927CT6GENIChomozygous68627067
103889103538891036AG20GENIChomozygous68358765
103889109038891091AC24GENIChomozygous68358767
103889118038891181GA17GENIChomozygous68627072
103889151038891510AG11GENIChomozygous69805298
103889168338891684CT16GENIChomozygous68358771
103889209738892098CG7GENIChomozygous68627076
103889251838892519GA6GENIChomozygous68627080
103889057838890579CT6GENIChomozygous69032750