| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69080351-69080464 | Rare:45 | ||||
| chr3:69084810-69085219 | Common:3; Rare:109 | ||||
| chr3:71065397-71065634 | Common:1; Rare:49 | ||||
| chr3:71130521-71130750 | Common:1; Rare:82; Clinvar:2 | ||||
| chr3:71130923-71131039 | Rare:17 | ||||
| chr3:71245065-71245204 | Common:1; Rare:33 | ||||
| chr3:71582253-71582356 | Rare:35 | ||||
| chr3:72848294-72848517 | Common:2; Rare:94 | ||||
| chr3:73624939-73625094 | Common:4; Rare:41 | ||||
| chr3:75785401-75785680 | Common:3; Rare:35 | ||||
| chr3:76311104-76311175 | Rare:21 | ||||
| chr3:79019011-79019059 | Rare:17 | ||||
| chr3:81761530-81761775 | Common:8; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:87227377-87227510 | Common:1; Rare:41; Clinvar (benign):1 | ||||
| chr3:88058827-88058859 | Common:1; Rare:7 |