| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:58045433-58046327 | Common:6; Rare:345 | ||||
| chr18:58247328-58247728 | Common:1; Rare:101 | ||||
| chr18:58671191-58671628 | Common:4; Rare:186; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:58862820-58863213 | Common:1; Rare:80 | ||||
| chr18:58863350-58863500 | Common:12; Rare:67 | ||||
| chr18:58863631-58863786 | Rare:46 | ||||
| chr18:58864473-58864644 | Common:1; Rare:26 | ||||
| chr18:58864752-58864915 | Rare:34 | ||||
| chr18:58865937-58866337 | Common:1; Rare:120 | ||||
| chr18:59139663-59139937 | Common:2; Rare:69 | ||||
| chr18:59358470-59358810 | Common:1; Rare:87 | ||||
| chr18:59359218-59359520 | Common:3; Rare:137; Clinvar:1 | ||||
| chr18:59899845-59899997 | Common:3; Rare:44 | ||||
| chr18:60372660-60373060 | Rare:112; Clinvar:2 | ||||
| chr18:61893538-61893827 | Common:2; Rare:70 |