In the ‘Genomic-region-based’ analysis, Cancer CRC can identify SEs by inputting the genomic regions, and then find the core TFs associated with these SEs. For these identified SEs, we also provide detailed annotation information, including commom SNPs, risk SNPs, and eQTLs.
Chromosome: Chromatin number of the entered genomic region.
Start position: Start position of the entered genomic region.
End position: End position of the entered genomic region.