Fig. 7From: Chromatin loop anchors are associated with genome instability in cancer and recombination hotspots in the germlineGenomic and epigenomic features influencing SNV and SV rates at loop anchor points in breast tumours. a, b Variable importance, measured as percentage increase in mean squared error (%IncMSE) when each predictor variable is removed from the model, predicting SNV rates (a) or SV breakpoint rates (b), respectively. c Spearman’s rank correlation coefficient estimates between mutation rates and predictor variables of the random forest models, for SNV rates (green) and SV breakpoint rates (blue); 95% confidence intervals of the estimates are indicated. d SNV rates in BRCA-EU breast tumours within 500 kb of LAPs in the MCF-7 breast tumour cell line relative to replication timing (average MCF-7 ENCODE Repli-seq signal); higher Repli-seq values indicate earlier replication timeBack to article page