| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33277342-33277489 | Common:1; Rare:36 | ||||
| chr3:33717983-33718182 | Rare:56 | ||||
| chr3:33798429-33798880 | Common:3; Rare:147 | ||||
| chr3:33798971-33799033 | Rare:20 | ||||
| chr3:36908430-36908646 | Common:1; Rare:46 | ||||
| chr3:36993078-36993607 | Common:2; Rare:189; Clinvar:39; Clinvar (benign):18; Clinvar (pathogenic):4 | ||||
| chr3:37176100-37176389 | Common:1; Rare:78 | ||||
| chr3:37243166-37243487 | Common:1; Rare:79 | ||||
| chr3:37987875-37988099 | Common:2; Rare:38 | ||||
| chr3:37990648-37990812 | Common:1; Rare:30 | ||||
| chr3:37992773-37993052 | Rare:34 | ||||
| chr3:38008149-38008329 | Rare:62 | ||||
| chr3:38024420-38024680 | Common:1; Rare:95 | ||||
| chr3:38029605-38029844 | Common:1; Rare:47 | ||||
| chr3:38038914-38039228 | Rare:59 |