| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33277325-33277482 | Common:1; Rare:41 | ||||
| chr3:33798290-33798706 | Common:3; Rare:123 | ||||
| chr3:33798997-33799049 | Rare:18 | ||||
| chr3:36993078-36993572 | Common:2; Rare:171; Clinvar:28; Clinvar (benign):14; Clinvar (pathogenic):3 | ||||
| chr3:37243166-37243365 | Common:1; Rare:50 | ||||
| chr3:38029612-38029780 | Common:1; Rare:33 | ||||
| chr3:38138574-38138718 | Common:2; Rare:57; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39051950-39052057 | Common:1; Rare:39 | ||||
| chr3:39107562-39107708 | Common:3; Rare:46 | ||||
| chr3:39153448-39153726 | Common:3; Rare:92 | ||||
| chr3:39383336-39383661 | Common:3; Rare:73; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:40309448-40309808 | Common:9; Rare:123 | ||||
| chr3:40457201-40457403 | Common:3; Rare:100 | ||||
| chr3:40505932-40506122 | Rare:43 | ||||
| chr3:41238966-41239353 | Common:1; Rare:127; Clinvar (benign):2 |