| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35240917-35241069 | Common:2; Rare:52 | ||||
| chr18:35290205-35290383 | Common:1; Rare:65 | ||||
| chr18:36129772-36129939 | Common:1; Rare:68 | ||||
| chr18:36828681-36829138 | Common:3; Rare:166 | ||||
| chr18:45967249-45967510 | Rare:98 | ||||
| chr18:46104136-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:47150452-47150546 | Common:2; Rare:34 | ||||
| chr18:48538996-48539208 | Common:1; Rare:50 | ||||
| chr18:49813826-49814087 | Common:1; Rare:112 | ||||
| chr18:50878921-50879235 | Common:4; Rare:107 | ||||
| chr18:55321786-55321921 | Rare:28 | ||||
| chr18:55589776-55590004 | Common:2; Rare:84 | ||||
| chr18:56651133-56651388 | Common:3; Rare:63 | ||||
| chr18:59139692-59139937 | Common:2; Rare:63 | ||||
| chr18:59697660-59697846 | Common:1; Rare:48 |