| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128957265-128957576 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:129033645-129033897 | Common:1; Rare:40 | ||||
| chr7:129403912-129403963 | Rare:7 | ||||
| chr7:129460925-129461206 | Common:1; Rare:40 | ||||
| chr7:129461350-129461486 | Rare:24 | ||||
| chr7:129634129-129634474 | Common:4; Rare:52 | ||||
| chr7:129728501-129728775 | Common:1; Rare:54 | ||||
| chr7:129815258-129815287 | Common:1; Rare:6 | ||||
| chr7:129817641-129817744 | Rare:18 | ||||
| chr7:129848119-129848237 | Rare:29 | ||||
| chr7:129848538-129848578 | Rare:7 | ||||
| chr7:129850395-129850462 | Rare:12 | ||||
| chr7:129949397-129949685 | Common:1; Rare:54 | ||||
| chr7:129949868-129949916 | Common:2; Rare:9 | ||||
| chr7:129950547-129950630 | Rare:23 |