| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74597790-74597920 | Common:1; Rare:35 | ||||
| chr18:75209056-75209240 | Common:1; Rare:65 | ||||
| chr18:75210688-75210905 | Common:3; Rare:53; Clinvar:7 | ||||
| chr18:76495173-76495506 | Common:2; Rare:90 | ||||
| chr18:76822227-76822636 | Common:11; Rare:115 | ||||
| chr18:77087441-77087529 | Common:4; Rare:26 | ||||
| chr18:77087569-77087694 | Common:1; Rare:27 | ||||
| chr18:77132630-77132798 | Common:2; Rare:50 | ||||
| chr18:79068974-79069304 | Common:8; Rare:142 | ||||
| chr18:79400092-79400331 | Common:3; Rare:80 | ||||
| chr18:79679140-79679587 | Common:3; Rare:197 | ||||
| chr18:79964558-79964742 | Common:2; Rare:54 | ||||
| chr18:79988249-79988651 | Common:3; Rare:127; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344786-344933 | Common:3; Rare:48 | ||||
| chr19:507817-508025 | Common:2; Rare:67 |