| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:21751091-21751405 | Common:4; Rare:99 | ||||
| chr3:23806953-23807275 | Common:1; Rare:87 | ||||
| chr3:23916911-23917214 | Rare:115 | ||||
| chr3:23917605-23917972 | Common:2; Rare:99; Clinvar (benign):1 | ||||
| chr3:25428107-25428398 | Rare:66 | ||||
| chr3:28348762-28349179 | Common:3; Rare:136 | ||||
| chr3:29280852-29281082 | Common:3; Rare:43 | ||||
| chr3:29281297-29281433 | Common:2; Rare:27 | ||||
| chr3:30606345-30606521 | Common:1; Rare:41; Clinvar:1 | ||||
| chr3:30606651-30606976 | Common:1; Rare:101; Clinvar:6; Clinvar (benign):6 | ||||
| chr3:31532381-31532638 | Common:2; Rare:71 | ||||
| chr3:32502747-32502949 | Rare:60 | ||||
| chr3:32685085-32685361 | Rare:81 | ||||
| chr3:33277303-33277501 | Common:2; Rare:54 | ||||
| chr3:33798514-33798690 | Common:2; Rare:63 |