| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:72867599-72867831 | Common:1; Rare:82 | ||||
| chr18:72868223-72868370 | Rare:58 | ||||
| chr18:74147820-74147923 | Common:8; Rare:68 | ||||
| chr18:74148352-74148590 | Common:1; Rare:72 | ||||
| chr18:74291871-74292301 | Common:5; Rare:128 | ||||
| chr18:74496029-74496434 | Common:4; Rare:128 | ||||
| chr18:74597566-74597929 | Common:2; Rare:100 | ||||
| chr18:76495167-76495529 | Common:2; Rare:94 | ||||
| chr18:76822220-76822591 | Common:11; Rare:104 | ||||
| chr18:79679193-79679568 | Common:3; Rare:171 | ||||
| chr18:79988262-79988689 | Common:4; Rare:139; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344784-344955 | Common:3; Rare:62 | ||||
| chr19:572237-572618 | Common:3; Rare:186 | ||||
| chr19:633508-633738 | Common:8; Rare:109 | ||||
| chr19:663126-663436 | Common:3; Rare:125 |