| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:25352072-25352406 | Common:2; Rare:135 | ||||
| chr18:31498062-31498254 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):4 | ||||
| chr18:32018745-32018860 | Common:1; Rare:33 | ||||
| chr18:35240912-35241094 | Common:2; Rare:69 | ||||
| chr18:35290148-35290384 | Common:2; Rare:75 | ||||
| chr18:35497880-35498086 | Common:2; Rare:62 | ||||
| chr18:35972465-35972763 | Common:3; Rare:103 | ||||
| chr18:36129223-36129473 | Common:4; Rare:76 | ||||
| chr18:36129812-36129928 | Rare:46 | ||||
| chr18:36187388-36187516 | Common:1; Rare:47 | ||||
| chr18:36828748-36829140 | Common:3; Rare:145 | ||||
| chr18:46098206-46098571 | Common:11; Rare:110; Clinvar (benign):6 | ||||
| chr18:46104135-46104406 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr18:48538996-48539287 | Common:2; Rare:64 | ||||
| chr18:49487143-49487332 | Common:3; Rare:77 |