| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:11908250-11908456 | Rare:64 | ||||
| chr18:12407757-12407969 | Common:5; Rare:87 | ||||
| chr18:12702612-12703094 | Common:3; Rare:190 | ||||
| chr18:12884148-12884405 | Common:4; Rare:131 | ||||
| chr18:12947701-12948098 | Common:3; Rare:109 | ||||
| chr18:12991137-12991390 | Common:1; Rare:91 | ||||
| chr18:13612510-13612622 | Common:2; Rare:29 | ||||
| chr18:13726439-13726729 | Common:3; Rare:112 | ||||
| chr18:14132405-14132666 | Common:3; Rare:67 | ||||
| chr18:21242196-21242334 | Common:1; Rare:55 | ||||
| chr18:21600632-21600815 | Rare:46 | ||||
| chr18:22933260-22933413 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr18:22933781-22933889 | Common:1; Rare:43 | ||||
| chr18:23453036-23453342 | Rare:103 | ||||
| chr18:23586416-23586563 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):1 |