| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31498062-31498259 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):5 | ||||
| chr18:31943095-31943397 | Common:7; Rare:101 | ||||
| chr18:32092390-32092706 | Common:4; Rare:140 | ||||
| chr18:34976942-34977067 | Common:1; Rare:22 | ||||
| chr18:35240912-35241100 | Common:2; Rare:72 | ||||
| chr18:35290193-35290384 | Common:2; Rare:68 | ||||
| chr18:35344394-35344524 | Common:2; Rare:41 | ||||
| chr18:35972449-35972713 | Common:4; Rare:81 | ||||
| chr18:36129309-36129471 | Common:1; Rare:45 | ||||
| chr18:36129829-36129928 | Rare:41 | ||||
| chr18:36187451-36187525 | Common:2; Rare:33 | ||||
| chr18:36828757-36829164 | Common:3; Rare:158 | ||||
| chr18:45967261-45967508 | Rare:92 | ||||
| chr18:46098228-46098550 | Common:11; Rare:93; Clinvar (benign):6 | ||||
| chr18:46104135-46104396 | Common:3; Rare:74; Clinvar (benign):1 |