chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14104341358104341359TC5GENIChomozygous113615430
14104342704104342705AG10GENIChomozygous114202595
14104349167104349168TC4GENIChomozygous113529811
14104346650104346651AG7GENIChomozygous113529805
14104347687104347688CA4GENIChomozygous113529807
14104348357104348358CT4GENIChomozygous113529809
14104349320104349321TC4GENIChomozygous113529813
14104349489104349490AG4GENIChomozygous113529815
14104350007104350008AT3GENIChomozygous113529819
14104351930104351931GT5GENIChomozygous113529821
14104352444104352445CT3GENIChomozygous113529823
14104352782104352783CT2GENIChomozygous113529825
14104353275104353276CT9GENIChomozygous113529827
14104357913104357914TC6GENIChomozygous113529829
14104358075104358076AG4GENIChomozygous113529831
14104360081104360082AG9GENIChomozygous113529833
14104360210104360211CA9GENIChomozygous113529835
14104363996104363997CA5GENIChomozygous113529841
14104364572104364573GA3GENIChomozygous113529843
14104365472104365473AG4GENIChomozygous113529845
14104366698104366699TC5GENIChomozygous113529847
14104370018104370019CA4GENIChomozygous113529849
14104370319104370320TC5GENIChomozygous113529851
14104371398104371399CT7GENIChomozygous113529857
14104371861104371862CG4GENIChomozygous113529861
14104371900104371901CT3GENIChomozygous113529863
14104373704104373705AT6GENICheterozygous113615433