chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122069060320690604AT12GENIChomozygous139107830
122069112620691127TC18GENIChomozygous139107832
122069135820691359CT13GENIChomozygous139107833
122069160120691602TC18GENIChomozygous139107834
122069276120692762C11GENIChomozygous139046285
122069384020693843GAA12GENIChomozygous139046286
122069599520695995AAAAAA14GENIChomozygous139046288
122069699820696999TC18GENIChomozygous139107842
122069700920697010TC18GENIChomozygous139107843
122069724520697246GC19GENIChomozygous142322681
122069103320691034TC10GENIChomozygous142322677
122069519620695197CT11GENIChomozygous142322678
122069582320695824AC12GENIChomozygous142322679
122069586320695864CT18GENIChomozygous142322680
122069277720692777G10GENIChomozygous142310099
122069601520696016CA15GENIChomozygous403320316
122069601520696016C15GENICheterozygous403320317