| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:9546035-9546366 | Common:8; Rare:79 | ||||
| chr5:9546401-9546523 | Common:3; Rare:21 | ||||
| chr5:10249862-10250435 | Common:19; Rare:268; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10307580-10307931 | Common:1; Rare:77 | ||||
| chr5:10353597-10353920 | Common:3; Rare:116 | ||||
| chr5:10354036-10354372 | Rare:114 | ||||
| chr5:10761015-10761497 | Common:15; Rare:166 | ||||
| chr5:14143206-14143366 | Rare:54 | ||||
| chr5:14143483-14143873 | Common:1; Rare:118; Clinvar:1 | ||||
| chr5:14340694-14340853 | Common:2; Rare:31 | ||||
| chr5:16465702-16465873 | Rare:30 | ||||
| chr5:16935961-16936447 | Common:3; Rare:135 | ||||
| chr5:17217325-17217669 | Common:3; Rare:57 | ||||
| chr5:31193552-31193863 | Common:1; Rare:65 | ||||
| chr5:31484795-31484951 | Rare:30 |