| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:122886120-122886350 | Rare:92 | ||||
| chr7:122886382-122886848 | Common:2; Rare:186 | ||||
| chr7:123748738-123749281 | Common:6; Rare:329 | ||||
| chr7:124929775-124930018 | Common:5; Rare:117 | ||||
| chr7:127392662-127392833 | Common:2; Rare:81 | ||||
| chr7:127585537-127585689 | Common:4; Rare:117 | ||||
| chr7:127588268-127588489 | Rare:154 | ||||
| chr7:127588930-127589200 | Rare:140 | ||||
| chr7:127651762-127652356 | Common:6; Rare:334 | ||||
| chr7:127686251-127686790 | Rare:213 | ||||
| chr7:128409928-128410064 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455722-128455926 | Common:4; Rare:223 | ||||
| chr7:128476667-128476875 | Rare:161 | ||||
| chr7:128739053-128739440 | Common:5; Rare:189 | ||||
| chr7:129054841-129055267 | Common:4; Rare:174 |