| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:29280893-29281081 | Common:2; Rare:35 | ||||
| chr3:32502775-32502912 | Rare:42 | ||||
| chr3:33097090-33097258 | Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277313-33277489 | Common:1; Rare:46 | ||||
| chr3:33798278-33798686 | Common:3; Rare:117 | ||||
| chr3:36993117-36993559 | Common:2; Rare:138; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37243162-37243348 | Common:1; Rare:49 | ||||
| chr3:38029626-38029867 | Common:1; Rare:48 | ||||
| chr3:39051944-39052025 | Common:1; Rare:30 | ||||
| chr3:39107562-39107716 | Common:3; Rare:49 | ||||
| chr3:39383324-39383653 | Common:3; Rare:76; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:40309512-40309808 | Common:8; Rare:105 | ||||
| chr3:40457213-40457388 | Common:3; Rare:87 | ||||
| chr3:42590735-42590903 | Common:2; Rare:53 | ||||
| chr3:42600377-42600709 | Common:2; Rare:130 |