| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:48410281-48410409 | Common:3; Rare:34 | ||||
| chr18:48538998-48539287 | Common:2; Rare:62 | ||||
| chr18:49116166-49116314 | Rare:23 | ||||
| chr18:49460506-49460740 | Common:1; Rare:65; Clinvar:7; Clinvar (benign):1 | ||||
| chr18:49487081-49487389 | Common:4; Rare:119 | ||||
| chr18:49490501-49490924 | Common:1; Rare:105 | ||||
| chr18:49492351-49492570 | Common:1; Rare:91 | ||||
| chr18:49561879-49562100 | Rare:57 | ||||
| chr18:49813151-49813477 | Common:3; Rare:66 | ||||
| chr18:49813489-49813638 | Rare:34 | ||||
| chr18:49813819-49814303 | Common:2; Rare:195 | ||||
| chr18:49879354-49879392 | Rare:7 | ||||
| chr18:50097569-50097723 | Common:1; Rare:24 | ||||
| chr18:50266325-50266559 | Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:50281415-50281840 | Common:3; Rare:132 |