| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:21427814-21428136 | Common:5; Rare:197 | ||||
| chr7:22356010-22356460 | Common:1; Rare:146 | ||||
| chr7:22357048-22357340 | Rare:171 | ||||
| chr7:22822748-22822957 | Common:6; Rare:152 | ||||
| chr7:23105644-23106025 | Common:7; Rare:263; Clinvar:7; Clinvar (benign):6 | ||||
| chr7:23181809-23182175 | Common:4; Rare:270 | ||||
| chr7:23273140-23273342 | Common:1; Rare:44 | ||||
| chr7:23299134-23299421 | Common:6; Rare:253 | ||||
| chr7:23307251-23308150 | Common:13; Rare:247 | ||||
| chr7:23467670-23468180 | Common:5; Rare:169 | ||||
| chr7:23468261-23468562 | Rare:86 | ||||
| chr7:23469269-23469434 | Common:1; Rare:58 | ||||
| chr7:23470298-23470612 | Common:2; Rare:178 | ||||
| chr7:23531952-23532112 | Common:1; Rare:110 | ||||
| chr7:23597235-23597505 | Common:2; Rare:156 |