| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:25352040-25352410 | Common:2; Rare:144 | ||||
| chr18:26546938-26547051 | Rare:34 | ||||
| chr18:28176968-28177308 | Common:3; Rare:163 | ||||
| chr18:31101241-31101632 | Common:11; Rare:104 | ||||
| chr18:31101910-31102068 | Common:1; Rare:39; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr18:31498118-31498337 | Common:1; Rare:84; Clinvar:7; Clinvar (benign):7 | ||||
| chr18:31943098-31943352 | Common:7; Rare:78 | ||||
| chr18:32092426-32092721 | Common:4; Rare:136 | ||||
| chr18:34593283-34593420 | Rare:20 | ||||
| chr18:34976942-34977061 | Common:1; Rare:20 | ||||
| chr18:35240912-35241109 | Common:2; Rare:74 | ||||
| chr18:35290188-35290391 | Common:2; Rare:72 | ||||
| chr18:35972449-35972719 | Common:4; Rare:85 | ||||
| chr18:36129294-36129466 | Common:1; Rare:52 | ||||
| chr18:36828748-36829153 | Common:3; Rare:152 |