| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25789968-25790119 | Common:4; Rare:59 | ||||
| chr3:28348612-28348732 | Rare:29 | ||||
| chr3:28348765-28349185 | Common:3; Rare:135 | ||||
| chr3:29280897-29281081 | Common:2; Rare:35 | ||||
| chr3:31532371-31532648 | Common:3; Rare:78 | ||||
| chr3:31981625-31981826 | Common:1; Rare:53 | ||||
| chr3:32106425-32106714 | Common:3; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570636-32570920 | Rare:133 | ||||
| chr3:33097098-33097279 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33114508-33114524 | Common:1; Rare:5; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:33277325-33277489 | Common:1; Rare:42 | ||||
| chr3:33717983-33718295 | Rare:112 | ||||
| chr3:33798290-33798706 | Common:3; Rare:123 | ||||
| chr3:33798735-33798866 | Common:1; Rare:42 | ||||
| chr3:33798985-33799203 | Rare:68 |