| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22084646-22084823 | Rare:37 | ||||
| chr18:22168158-22168327 | Common:4; Rare:28 | ||||
| chr18:22168419-22168582 | Rare:37 | ||||
| chr18:22174311-22174586 | Common:3; Rare:48 | ||||
| chr18:22176723-22177021 | Common:1; Rare:68; Clinvar:1 | ||||
| chr18:22816381-22816532 | Rare:27 | ||||
| chr18:22839554-22839637 | Rare:14 | ||||
| chr18:31091999-31092191 | Common:1; Rare:46; Clinvar:7; Clinvar (benign):5 | ||||
| chr18:32216726-32217117 | Common:2; Rare:77 | ||||
| chr18:32221883-32222179 | Common:1; Rare:49 | ||||
| chr18:35478586-35478855 | Rare:42 | ||||
| chr18:48951855-48951914 | Common:1; Rare:19 | ||||
| chr18:49835344-49835517 | Rare:43 | ||||
| chr18:49847249-49847383 | Rare:39 | ||||
| chr18:49945439-49945519 | Common:1; Rare:14 |