chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224881521224881522CT17GENIChomozygous57112698
4224882730224882731C-21GENIChomozygous57112699
4224883229224883230C-25GENIChomozygous57112701
4224883609224883610CG23GENIChomozygous57112703
4224884028224884029GA22GENIChomozygous57112704
4224884079224884080C-21GENIChomozygous57112708
4224884722224884723GA11GENIChomozygous57112715
4224886425224886426GGGA2GENICheterozygous58448307
4224889201224889221TGTGTGTGTGTGTGTGTGTG--------------------12GENIChomozygous57112718
4224892234224892235AG24GENIChomozygous57112720
4224892649224892650AATCTTTTT12GENIChomozygous57112724
4224893211224893212GA41GENIChomozygous58023894
4224884101224884102TTTCCTCCTTCCTTCCTCCCTCCCTCTCCTCCTCCCTTACTCCTTCCCTCCCTCCC36GENIChomozygous58307134
4224886428224886429TG7GENIChomozygous58376692
4224886430224886431CG7GENIChomozygous58376694
4224886434224886435CG7GENIChomozygous58376696
4224886438224886439CG7GENIChomozygous58376698
4224886937224886938CCTGTGTGTGTG8GENICpossibly homozygous58376700