| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:27147771-27147985 | Rare:41 | ||||
| chr7:27150692-27151038 | Common:4; Rare:81 | ||||
| chr7:27156000-27156276 | Common:2; Rare:95 | ||||
| chr7:27662722-27663152 | Common:7; Rare:144 | ||||
| chr7:27740037-27740223 | Common:5; Rare:59 | ||||
| chr7:27863861-27863962 | Rare:14 | ||||
| chr7:28958301-28958479 | Rare:45 | ||||
| chr7:29194203-29194555 | Rare:97 | ||||
| chr7:29479977-29480338 | Common:2; Rare:112 | ||||
| chr7:30026620-30026928 | Rare:76 | ||||
| chr7:30504687-30505090 | Common:4; Rare:136 | ||||
| chr7:30594717-30594949 | Common:3; Rare:106; Clinvar:6; Clinvar (benign):6 | ||||
| chr7:30752033-30752291 | Common:4; Rare:66 | ||||
| chr7:30771304-30771537 | Common:1; Rare:81 | ||||
| chr7:32495240-32495607 | Common:1; Rare:94 |