| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63367122-63367354 | Common:1; Rare:87 | ||||
| chr18:63422370-63422694 | Common:2; Rare:94 | ||||
| chr18:63970032-63970148 | Common:2; Rare:24 | ||||
| chr18:67516701-67517033 | Common:5; Rare:86 | ||||
| chr18:68714960-68715262 | Common:7; Rare:133 | ||||
| chr18:70205659-70205783 | Common:3; Rare:51; Clinvar (benign):2 | ||||
| chr18:74148353-74148561 | Common:1; Rare:69 | ||||
| chr18:74291747-74292034 | Common:1; Rare:101; Clinvar:1 | ||||
| chr18:74496013-74496407 | Common:4; Rare:129 | ||||
| chr18:74499743-74499953 | Common:2; Rare:45 | ||||
| chr18:74597352-74597484 | Common:1; Rare:31 | ||||
| chr18:74597570-74597675 | Common:1; Rare:29 | ||||
| chr18:74597780-74597915 | Common:1; Rare:35 | ||||
| chr18:75209069-75209240 | Common:1; Rare:61 | ||||
| chr18:75210765-75210910 | Common:4; Rare:44; Clinvar:7; Clinvar (benign):1 |