| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23202929-23203213 | Common:1; Rare:99 | ||||
| chr3:23916887-23917230 | Rare:130 | ||||
| chr3:24494722-24495264 | Common:2; Rare:151 | ||||
| chr3:25428107-25428376 | Rare:59 | ||||
| chr3:25783358-25783621 | Common:2; Rare:95; Clinvar (benign):3 | ||||
| chr3:25790008-25790126 | Common:4; Rare:45 | ||||
| chr3:28291732-28291854 | Common:1; Rare:25 | ||||
| chr3:28348574-28348735 | Rare:33 | ||||
| chr3:28348784-28349185 | Common:3; Rare:126 | ||||
| chr3:29280887-29281407 | Common:14; Rare:99 | ||||
| chr3:31532385-31532662 | Common:4; Rare:79 | ||||
| chr3:31533016-31533293 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr3:32238537-32238706 | Common:2; Rare:54 | ||||
| chr3:32570718-32570919 | Rare:97 | ||||
| chr3:32818164-32818342 | Rare:77 |