| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:6729776-6729821 | Rare:13 | ||||
| chr18:9102475-9102766 | Common:2; Rare:118; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136542-9136843 | Rare:120 | ||||
| chr18:9334488-9334867 | Common:1; Rare:94 | ||||
| chr18:10525829-10526093 | Common:2; Rare:99 | ||||
| chr18:11851243-11851427 | Common:1; Rare:62 | ||||
| chr18:11908276-11908423 | Rare:42 | ||||
| chr18:12702660-12703099 | Common:3; Rare:176 | ||||
| chr18:12947703-12948049 | Common:3; Rare:77 | ||||
| chr18:12991125-12991403 | Common:2; Rare:105 | ||||
| chr18:13726503-13726724 | Common:3; Rare:82 | ||||
| chr18:21242195-21242400 | Common:1; Rare:83 | ||||
| chr18:21600625-21600921 | Common:2; Rare:79 | ||||
| chr18:21600952-21601218 | Rare:53 | ||||
| chr18:22933235-22933446 | Common:3; Rare:80; Clinvar:4; Clinvar (benign):2 |