| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:125916341-125916626 | Common:4; Rare:84 | ||||
| chr3:126356035-126356234 | Rare:53 | ||||
| chr3:127761192-127761477 | Common:3; Rare:46 | ||||
| chr3:130111461-130111707 | Common:3; Rare:64 | ||||
| chr3:130112409-130112547 | Common:2; Rare:33 | ||||
| chr3:131361582-131361927 | Common:3; Rare:103 | ||||
| chr3:133674467-133674574 | Common:2; Rare:18 | ||||
| chr3:133756707-133757021 | Common:5; Rare:97; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:135155871-135156004 | Rare:30 | ||||
| chr3:142936075-142936285 | Common:2; Rare:35 | ||||
| chr3:148701946-148702021 | Rare:12 | ||||
| chr3:148840585-148840756 | Common:2; Rare:48 | ||||
| chr3:149206166-149206603 | Common:3; Rare:102; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr3:149223926-149224268 | Common:4; Rare:59 | ||||
| chr3:150408860-150409020 | Rare:46 |