| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33798509-33798932 | Common:3; Rare:152 | ||||
| chr3:36993102-36993491 | Common:2; Rare:114; Clinvar:14; Clinvar (benign):6 | ||||
| chr3:37176108-37176381 | Common:1; Rare:71 | ||||
| chr3:37861712-37861891 | Common:1; Rare:41 | ||||
| chr3:38138576-38138701 | Common:2; Rare:50; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39107568-39107687 | Common:2; Rare:36 | ||||
| chr3:39383578-39383650 | Rare:17 | ||||
| chr3:44624953-44625086 | Common:2; Rare:41 | ||||
| chr3:44761600-44761794 | Common:3; Rare:67 | ||||
| chr3:44976122-44976275 | Common:2; Rare:64 | ||||
| chr3:45689177-45689455 | Common:1; Rare:93 | ||||
| chr3:48301367-48301466 | Common:1; Rare:21 | ||||
| chr3:48440011-48440299 | Common:2; Rare:105 | ||||
| chr3:48918726-48918900 | Common:2; Rare:93 | ||||
| chr3:49007181-49007429 | Common:2; Rare:97 |