| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:19946974-19947442 | Common:7; Rare:173 | ||||
| chr3:20186123-20186418 | Common:4; Rare:93 | ||||
| chr3:23202926-23203186 | Common:1; Rare:95 | ||||
| chr3:23805802-23806072 | Common:2; Rare:53 | ||||
| chr3:23916860-23917361 | Rare:171 | ||||
| chr3:24494762-24494909 | Rare:37 | ||||
| chr3:24495703-24495863 | Common:1; Rare:51 | ||||
| chr3:25428103-25428382 | Rare:62 | ||||
| chr3:25783388-25783641 | Common:2; Rare:81; Clinvar (benign):3 | ||||
| chr3:25790008-25790126 | Common:4; Rare:45 | ||||
| chr3:27194087-27194251 | Common:2; Rare:26 | ||||
| chr3:28241439-28241791 | Common:2; Rare:121 | ||||
| chr3:28348607-28348711 | Rare:24 | ||||
| chr3:28348773-28349178 | Common:3; Rare:130 | ||||
| chr3:28349625-28349859 | Rare:59 |