| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69013589-69013830 | Common:1; Rare:74 | ||||
| chr3:69080342-69080460 | Rare:51 | ||||
| chr3:69084818-69085221 | Common:3; Rare:110 | ||||
| chr3:69200881-69200986 | Common:1; Rare:24 | ||||
| chr3:69739190-69739523 | Rare:106 | ||||
| chr3:71130539-71130694 | Common:1; Rare:62; Clinvar:2 | ||||
| chr3:71245063-71245176 | Rare:28 | ||||
| chr3:71581921-71582158 | Common:1; Rare:55 | ||||
| chr3:72996715-72997061 | Common:2; Rare:127 | ||||
| chr3:73624129-73624499 | Common:6; Rare:110 | ||||
| chr3:73625255-73625417 | Common:1; Rare:32 | ||||
| chr3:75785492-75785694 | Common:3; Rare:25 | ||||
| chr3:79018995-79019053 | Rare:20 | ||||
| chr3:81761439-81761828 | Common:8; Rare:138; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:87227032-87227413 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):2 |