| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:24397758-24398061 | Common:2; Rare:112 | ||||
| chr18:24426609-24426785 | Common:3; Rare:66 | ||||
| chr18:25351056-25351129 | Rare:25 | ||||
| chr18:32092359-32092727 | Common:6; Rare:169 | ||||
| chr18:35240917-35241100 | Common:2; Rare:69 | ||||
| chr18:35290183-35290384 | Common:2; Rare:72 | ||||
| chr18:35344385-35344529 | Common:2; Rare:44 | ||||
| chr18:35972465-35972713 | Common:3; Rare:77 | ||||
| chr18:36129177-36129473 | Common:4; Rare:86 | ||||
| chr18:36129812-36129934 | Rare:51 | ||||
| chr18:36187377-36187516 | Common:1; Rare:51 | ||||
| chr18:36828748-36829164 | Common:3; Rare:163 | ||||
| chr18:37566041-37566277 | Common:6; Rare:65 | ||||
| chr18:46104135-46104406 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr18:46917412-46917634 | Common:2; Rare:90 |