Multiple-omics high-throughput sequencing has been used to identify several driver genes in ESCC, for example, mutations, deletions and amplifications of TP53, ZNF750, NOTCH1, NFE2L2, TP63 and SOX2 genes have frequently been identified in ESCC specimens, constituting the most common genomic features of ESCC [16,17]. This evidence concerns the gene ZNF750 and esophageal squamous cell carcinoma.