| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63970008-63970145 | Common:1; Rare:29 | ||||
| chr18:66603956-66604389 | Common:5; Rare:91 | ||||
| chr18:68714960-68715262 | Common:7; Rare:133 | ||||
| chr18:70205644-70205837 | Common:3; Rare:81; Clinvar (benign):2 | ||||
| chr18:70205964-70206153 | Rare:62 | ||||
| chr18:70288669-70289078 | Common:6; Rare:131 | ||||
| chr18:70296373-70296467 | Rare:23 | ||||
| chr18:74148352-74148604 | Common:1; Rare:75 | ||||
| chr18:74291906-74292281 | Common:4; Rare:112 | ||||
| chr18:74457117-74457422 | Common:4; Rare:99 | ||||
| chr18:74458093-74458417 | Common:1; Rare:76 | ||||
| chr18:74496021-74496434 | Common:4; Rare:132 | ||||
| chr18:74566960-74567072 | Rare:25 | ||||
| chr18:74597359-74597484 | Common:1; Rare:31 | ||||
| chr18:74597590-74597929 | Common:2; Rare:95 |