| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151519891-151520077 | Common:1; Rare:56 | ||||
| chr7:151736463-151736663 | Common:1; Rare:32 | ||||
| chr7:152113028-152113261 | Rare:42 | ||||
| chr7:152154865-152155230 | Rare:57 | ||||
| chr7:152676043-152676276 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):13 | ||||
| chr7:155003131-155003474 | Common:7; Rare:124 | ||||
| chr7:155298965-155299143 | Rare:34 | ||||
| chr7:155644348-155644728 | Common:2; Rare:133 | ||||
| chr7:156640551-156640916 | Common:4; Rare:149 | ||||
| chr7:156950126-156950385 | Common:2; Rare:117 | ||||
| chr7:157336746-157337016 | Common:2; Rare:115 | ||||
| chr7:158856425-158856746 | Common:7; Rare:114 | ||||
| chr8:232149-232403 | Common:3; Rare:99 | ||||
| chr8:1755606-1755764 | Common:3; Rare:50 | ||||
| chr8:1823768-1824093 | Common:9; Rare:120 |