| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21600625-21600946 | Common:2; Rare:87 | ||||
| chr18:21704679-21704932 | Common:3; Rare:88 | ||||
| chr18:22913940-22914275 | Rare:52 | ||||
| chr18:22933260-22933435 | Common:2; Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933767-22933889 | Common:1; Rare:47 | ||||
| chr18:23453169-23453353 | Rare:64 | ||||
| chr18:23586416-23586537 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24426620-24426775 | Common:3; Rare:62 | ||||
| chr18:25351009-25351129 | Rare:45 | ||||
| chr18:25352072-25352406 | Common:2; Rare:135 | ||||
| chr18:26546859-26546920 | Rare:23 | ||||
| chr18:26657374-26657481 | Rare:26 | ||||
| chr18:28176968-28177295 | Common:3; Rare:158 | ||||
| chr18:31101485-31101595 | Common:9; Rare:37 | ||||
| chr18:31101901-31102048 | Common:1; Rare:39; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |