| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:6729872-6729943 | Rare:22 | ||||
| chr18:9102519-9102765 | Common:1; Rare:101; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136603-9136882 | Rare:110 | ||||
| chr18:9708056-9708400 | Common:4; Rare:89 | ||||
| chr18:9914203-9914265 | Rare:35 | ||||
| chr18:11908267-11908456 | Rare:56 | ||||
| chr18:12702658-12703110 | Common:3; Rare:181 | ||||
| chr18:12884134-12884425 | Common:4; Rare:149 | ||||
| chr18:12947703-12948045 | Common:2; Rare:77 | ||||
| chr18:12991137-12991410 | Common:2; Rare:100 | ||||
| chr18:13726410-13726720 | Common:4; Rare:116 | ||||
| chr18:21111147-21111343 | Common:1; Rare:47 | ||||
| chr18:22913797-22914169 | Rare:64 | ||||
| chr18:22933797-22933903 | Common:1; Rare:42 | ||||
| chr18:23453177-23453345 | Rare:58 |