| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348602-28349179 | Common:3; Rare:174 | ||||
| chr3:29280837-29281099 | Common:3; Rare:55 | ||||
| chr3:31532362-31532641 | Common:2; Rare:81 | ||||
| chr3:32570763-32571014 | Common:1; Rare:110 | ||||
| chr3:33096755-33097084 | Common:3; Rare:106; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr3:33277233-33277495 | Common:2; Rare:67 | ||||
| chr3:33798558-33798662 | Common:2; Rare:39 | ||||
| chr3:36992723-36992943 | Rare:72 | ||||
| chr3:36993067-36993563 | Common:2; Rare:168; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37174551-37174796 | Common:5; Rare:30 | ||||
| chr3:37176059-37176398 | Common:1; Rare:95 | ||||
| chr3:37861716-37861963 | Common:1; Rare:53 | ||||
| chr3:38138610-38138707 | Common:2; Rare:42; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39107537-39107708 | Common:3; Rare:54 | ||||
| chr3:39383289-39383430 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 |