| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35497880-35498178 | Common:2; Rare:81 | ||||
| chr18:35972465-35972731 | Common:3; Rare:91 | ||||
| chr18:36129294-36129557 | Common:1; Rare:86 | ||||
| chr18:36129827-36129939 | Rare:51 | ||||
| chr18:36187416-36187525 | Common:2; Rare:42 | ||||
| chr18:36828742-36829148 | Common:3; Rare:155 | ||||
| chr18:45828922-45829091 | Rare:30 | ||||
| chr18:45967249-45967483 | Rare:83 | ||||
| chr18:46072165-46072432 | Common:2; Rare:68 | ||||
| chr18:46072454-46072604 | Common:1; Rare:38 | ||||
| chr18:46098183-46098362 | Common:4; Rare:81; Clinvar (benign):8 | ||||
| chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46917370-46917665 | Common:3; Rare:124 | ||||
| chr18:47150445-47150575 | Common:3; Rare:48 | ||||
| chr18:49460577-49460793 | Common:2; Rare:68; Clinvar:4; Clinvar (benign):1 |