Fig. 3

circRNAs mapped to the 1000 Genomes Project and the clinVAR database. a The chromosome distribution of common variants from the 1000 Genomes Project. SNP: single nucleotide polymorphism; MNP: multiple nucleotide polymorphism; INDEL: insertion and deletion; SV: structure variant. The orange line is the ratio between the number of circRNA variants from the 1000 Genomes Project and the length of the chromosome. b The chromosome distribution of circRNA variants with phenotypes from the clinVAR database. The orange line is the ratio between the number of circRNA variants from the ClinVAR database and the length of the chromosome