| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33439516-33440042 | Common:5; Rare:277 | ||||
| chr3:33440102-33441801 | Common:22; Rare:1010 | ||||
| chr3:33717720-33717900 | Common:1; Rare:53 | ||||
| chr3:33718040-33718400 | Rare:199 | ||||
| chr3:33798150-33798360 | Common:3; Rare:44 | ||||
| chr3:33798435-33798703 | Common:6; Rare:221 | ||||
| chr3:33798856-33799133 | Rare:152 | ||||
| chr3:36944828-36945175 | Common:2; Rare:124 | ||||
| chr3:36992992-36993613 | Common:6; Rare:570; Clinvar:100; Clinvar (benign):44; Clinvar (pathogenic):10 | ||||
| chr3:36993663-36993880 | Rare:137; Clinvar:4; Clinvar (benign):3 | ||||
| chr3:37174290-37175006 | Common:5; Rare:147 | ||||
| chr3:37175465-37176606 | Common:8; Rare:494 | ||||
| chr3:37176668-37177043 | Common:12; Rare:162 | ||||
| chr3:37243070-37243498 | Common:10; Rare:273 | ||||
| chr3:37243549-37243767 | Common:4; Rare:140 |