| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:150379070-150379362 | Common:1; Rare:105 | ||||
| chr7:150450538-150450876 | Common:1; Rare:75 | ||||
| chr7:151028149-151028512 | Rare:136 | ||||
| chr7:151080793-151080980 | Rare:62 | ||||
| chr7:151736463-151736621 | Rare:25 | ||||
| chr7:155644377-155644734 | Common:2; Rare:121 | ||||
| chr7:156640537-156640781 | Common:3; Rare:116 | ||||
| chr7:157336776-157337101 | Common:3; Rare:156; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158704737-158704928 | Common:1; Rare:69 | ||||
| chr7:158856441-158856685 | Common:7; Rare:88 | ||||
| chr8:232139-232382 | Common:3; Rare:98 | ||||
| chr8:233054-233409 | Common:1; Rare:74 | ||||
| chr8:6406518-6406689 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6562645-6563472 | Common:6; Rare:231 | ||||
| chr8:6563516-6563552 | Rare:9 |