| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69013635-69013756 | Rare:33 | ||||
| chr3:69052229-69052429 | Common:3; Rare:72 | ||||
| chr3:69084776-69085063 | Common:3; Rare:75 | ||||
| chr3:81761515-81761698 | Common:7; Rare:64; Clinvar (benign):1 | ||||
| chr3:87227189-87227343 | Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058932-88059268 | Common:3; Rare:110 | ||||
| chr3:88149902-88150064 | Common:5; Rare:71 | ||||
| chr3:94062910-94063040 | Rare:35 | ||||
| chr3:97764439-97764795 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr3:98732429-98732508 | Rare:15 | ||||
| chr3:98901640-98901973 | Common:1; Rare:124 | ||||
| chr3:99638328-99638624 | Common:1; Rare:63 | ||||
| chr3:99817592-99817915 | Rare:95 | ||||
| chr3:99876116-99876317 | Common:1; Rare:54 | ||||
| chr3:100260733-100261028 | Rare:75 |