| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22933781-22933889 | Common:1; Rare:43 | ||||
| chr18:23453172-23453353 | Rare:62 | ||||
| chr18:23503320-23503542 | Common:1; Rare:78 | ||||
| chr18:23586408-23586531 | Common:2; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24397795-24397987 | Common:2; Rare:80 | ||||
| chr18:24426384-24426758 | Common:5; Rare:139 | ||||
| chr18:26133781-26133863 | Common:1; Rare:20 | ||||
| chr18:28177006-28177133 | Common:3; Rare:69 | ||||
| chr18:31498069-31498329 | Common:1; Rare:95; Clinvar:8; Clinvar (benign):7 | ||||
| chr18:31943098-31943375 | Common:7; Rare:89 | ||||
| chr18:32091842-32091997 | Common:3; Rare:58 | ||||
| chr18:32092388-32092706 | Common:4; Rare:142 | ||||
| chr18:33440800-33440877 | Rare:31 | ||||
| chr18:34976934-34977061 | Common:1; Rare:22 | ||||
| chr18:35041283-35041454 | Rare:68 |