| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:61251370-61251586 | Common:4; Rare:53 | ||||
| chr3:62318890-62319062 | Rare:71 | ||||
| chr3:63863779-63864150 | Common:7; Rare:123 | ||||
| chr3:63864452-63864583 | Common:2; Rare:46 | ||||
| chr3:64018817-64019315 | Common:4; Rare:117 | ||||
| chr3:71725194-71725520 | Common:2; Rare:114 | ||||
| chr3:71755050-71755182 | Rare:32 | ||||
| chr3:87227172-87227334 | Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058914-88059313 | Common:3; Rare:151 | ||||
| chr3:88149641-88149675 | Rare:5 | ||||
| chr3:88149812-88150027 | Rare:66 | ||||
| chr3:94062961-94063061 | Rare:23 | ||||
| chr3:98593603-98593753 | Common:1; Rare:59 | ||||
| chr3:100401398-100401567 | Common:1; Rare:31 | ||||
| chr3:101513154-101513217 | Common:6; Rare:19 |