chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122069060320690604AT33GENIChomozygous139107830
122069112620691127TC33GENIChomozygous139107832
122069135820691359CT47GENIChomozygous139107833
122069160120691602TC39GENIChomozygous139107834
122069276120692762C36GENIChomozygous139046285
122069384020693843GAA46GENIChomozygous139046286
122069599520695995AAAAAA19GENIChomozygous139046288
122069699820696999TC39GENIChomozygous139107842
122069700920697010TC39GENIChomozygous139107843
122069103320691034TC29GENIChomozygous142322677
122069519620695197CT40GENIChomozygous142322678
122069582320695824AC32GENICpossibly homozygous142322679
122069586320695864CT35GENIChomozygous142322680
122069724520697246GC45GENIChomozygous142322681
122069277720692777G34GENIChomozygous142310099
122069601520696016C20GENICheterozygous403320317
122069601520696016CA20GENIChomozygous403320316