| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23916911-23917199 | Rare:109 | ||||
| chr3:25783392-25783641 | Common:2; Rare:78; Clinvar (benign):3 | ||||
| chr3:28348985-28349178 | Common:2; Rare:59 | ||||
| chr3:29280991-29281076 | Common:1; Rare:12 | ||||
| chr3:31532371-31532638 | Common:2; Rare:76 | ||||
| chr3:32106353-32106667 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570766-32570958 | Common:1; Rare:87 | ||||
| chr3:33097104-33097217 | Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277306-33277489 | Common:1; Rare:47 | ||||
| chr3:33798434-33798662 | Common:2; Rare:72 | ||||
| chr3:36993166-36993557 | Common:2; Rare:118; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37243166-37243361 | Common:1; Rare:49 | ||||
| chr3:39051962-39052042 | Common:1; Rare:27 | ||||
| chr3:39107597-39107681 | Common:2; Rare:26 | ||||
| chr3:39406579-39406764 | Common:2; Rare:78 |