| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:123601600-123601858 | Rare:61 | ||||
| chr7:123748661-123749285 | Common:4; Rare:222 | ||||
| chr7:124929793-124930007 | Common:3; Rare:68 | ||||
| chr7:127392071-127392324 | Rare:98 | ||||
| chr7:127585281-127585443 | Common:1; Rare:36 | ||||
| chr7:127585552-127585694 | Common:2; Rare:55 | ||||
| chr7:127588265-127588496 | Rare:98 | ||||
| chr7:127588917-127589090 | Rare:53 | ||||
| chr7:127651820-127652231 | Common:3; Rare:119 | ||||
| chr7:127990710-127991021 | Rare:61 | ||||
| chr7:128409920-128410044 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455729-128455954 | Common:2; Rare:123 | ||||
| chr7:128791232-128791496 | Common:2; Rare:66 | ||||
| chr7:128830193-128830422 | Common:2; Rare:60 | ||||
| chr7:129054762-129055239 | Common:2; Rare:110; Clinvar (benign):2 |