| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:6729815-6729923 | Rare:28 | ||||
| chr18:9102441-9102766 | Common:2; Rare:134; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136544-9136851 | Rare:120 | ||||
| chr18:9708057-9708349 | Common:4; Rare:71 | ||||
| chr18:9914203-9914265 | Rare:35 | ||||
| chr18:11908266-11908431 | Rare:48 | ||||
| chr18:12702678-12703090 | Common:3; Rare:167 | ||||
| chr18:12947691-12948045 | Common:2; Rare:84 | ||||
| chr18:12991168-12991431 | Common:2; Rare:91 | ||||
| chr18:13726490-13726720 | Common:3; Rare:88 | ||||
| chr18:21600633-21600847 | Rare:52 | ||||
| chr18:22933289-22933401 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:22933807-22933867 | Common:1; Rare:23 | ||||
| chr18:23586416-23586678 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:25352092-25352410 | Common:2; Rare:129 |