LINC01488 was also detected in a long-range interaction with CCND1 (Fig. 5h) and showed significant correlation to CCND1 expression in both SCAN-B (Fig. 5i) and the TCGA-BRCA cohort (Supplementary Fig. 13). This evidence concerns the gene CCND1 and spinocerebellar ataxia, autosomal recessive, with axonal neuropathy.