| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:29280843-29280911 | Common:1; Rare:12 | ||||
| chr3:29280991-29281417 | Common:13; Rare:78 | ||||
| chr3:31532371-31532662 | Common:4; Rare:86 | ||||
| chr3:31532939-31533293 | Common:2; Rare:128; Clinvar (benign):2 | ||||
| chr3:31981634-31981788 | Common:1; Rare:40 | ||||
| chr3:32106378-32106697 | Common:4; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32391756-32391967 | Common:3; Rare:56 | ||||
| chr3:32502741-32502902 | Rare:53 | ||||
| chr3:32570636-32571043 | Common:1; Rare:177 | ||||
| chr3:32685167-32685361 | Rare:57 | ||||
| chr3:33096761-33096864 | Rare:32 | ||||
| chr3:33097078-33097300 | Common:3; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:33277289-33277490 | Common:2; Rare:54 | ||||
| chr3:33440856-33441088 | Common:2; Rare:49 | ||||
| chr3:33798435-33798686 | Common:2; Rare:81 |