| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:29280777-29281102 | Common:4; Rare:65 | ||||
| chr3:29281325-29281648 | Common:2; Rare:65 | ||||
| chr3:30606599-30606968 | Common:1; Rare:114; Clinvar:6; Clinvar (benign):6 | ||||
| chr3:31532380-31532624 | Common:2; Rare:68 | ||||
| chr3:31532864-31533261 | Common:3; Rare:156; Clinvar (benign):2 | ||||
| chr3:31981192-31981428 | Common:2; Rare:48 | ||||
| chr3:32106415-32106706 | Common:4; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502729-32502905 | Rare:53 | ||||
| chr3:32570752-32570994 | Common:1; Rare:102 | ||||
| chr3:32685396-32685473 | Rare:17 | ||||
| chr3:33046229-33046498 | Common:3; Rare:51 | ||||
| chr3:33096735-33097081 | Common:3; Rare:107; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr3:33097104-33097285 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33114129-33114501 | Common:1; Rare:151; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:33114504-33114545 | Common:1; Rare:14; Clinvar:3; Clinvar (benign):1 |