| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74254360-74254568 | Rare:97 | ||||
| chr7:74657500-74657730 | Common:2; Rare:68 | ||||
| chr7:74657944-74658067 | Common:1; Rare:27 | ||||
| chr7:74684611-74684692 | Common:1; Rare:19 | ||||
| chr7:74727874-74728028 | Common:1; Rare:29 | ||||
| chr7:75073441-75073823 | Common:4; Rare:121 | ||||
| chr7:75395338-75395491 | Rare:28 | ||||
| chr7:75442794-75442835 | Rare:13 | ||||
| chr7:75486226-75486596 | Common:2; Rare:118 | ||||
| chr7:75493696-75493940 | Common:3; Rare:41 | ||||
| chr7:75563342-75563458 | Rare:13 | ||||
| chr7:75611754-75611898 | Common:1; Rare:28 | ||||
| chr7:75878805-75879094 | Common:12; Rare:104 | ||||
| chr7:75914917-75915176 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75992537-75992739 | Common:3; Rare:50 |